US20060020281A1 - Valve assembly including diameter reduction structure for trocar - Google Patents
Valve assembly including diameter reduction structure for trocar Download PDFInfo
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- US20060020281A1 US20060020281A1 US11/097,550 US9755005A US2006020281A1 US 20060020281 A1 US20060020281 A1 US 20060020281A1 US 9755005 A US9755005 A US 9755005A US 2006020281 A1 US2006020281 A1 US 2006020281A1
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- Prior art keywords
- seal
- housing
- surgical
- diameter reduction
- locking
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/34—Trocars; Puncturing needles
- A61B17/3462—Trocars; Puncturing needles with means for changing the diameter or the orientation of the entrance port of the cannula, e.g. for use with different-sized instruments, reduction ports, adapter seals
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00477—Coupling
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/34—Trocars; Puncturing needles
- A61B17/3462—Trocars; Puncturing needles with means for changing the diameter or the orientation of the entrance port of the cannula, e.g. for use with different-sized instruments, reduction ports, adapter seals
- A61B2017/3464—Trocars; Puncturing needles with means for changing the diameter or the orientation of the entrance port of the cannula, e.g. for use with different-sized instruments, reduction ports, adapter seals with means acting on inner surface of valve or seal for expanding or protecting, e.g. inner pivoting fingers
Abstract
A surgical seal assembly includes a sleeve housing adapted to be operatively connected to a surgical sleeve, a seal housing adapted for releasable mounting to the sleeve housing and having a seal member with inner portions adapted to permit passage of a surgical object in substantial sealed relation therewith, and a manual lock member associated with the sleeve housing. The manual lock member is adapted for movement relative to the seal housing between a first position corresponding to a release position of the seal housing to permit removal of the seal housing from mounting to the sleeve housing and a second position corresponding to a lock position of the seal housing to secure the seal housing to the sleeve housing. The manual lock member is preferably adapted for rotational movement relative to a longitudinal axis of the seal housing to move between the first and second positions thereof.
Description
- This application is a continuation-in-part of U.S. patent application Ser. No. 10/380,942, which is a national phase application of International Application No. PCT/US01/31911, filed Oct. 12, 2001, which claims priority to U.S. Application Ser. No. 60/240,506, filed Oct. 13, 2000, the entire contents of each application being hereby incorporated by their entireties by reference herein.
- 1. Technical Field
- The present disclosure relates to a mechanism for controlling the operable inside diameter of a passageway through a valve assembly of a trocar housing. More particularly, the present disclosure relates to a diameter reduction structure that restricts the movement of small surgical instruments and. accommodates large diameter surgical instruments in the passageway of a trocar housing to facilitate the maintenance of a gas tight seal formed by the valve assembly.
- 2. Background of Related Art
- Trocar valve assemblies preferably provide a fluid tight seal about a surgical instrument introduced through the trocar during a minimally invasive surgical procedure. A typical valve assembly includes an outer seal, which can be fixed or floating, in combination with additional inner seals. Fixed outer seals are limited by their ability to sustain a seal when a smaller surgical instrument is moved off-axis relative to a central axis of the trocar. Fixed seals are also limited by their ability to sustain their integrity when the surgical instrument is angulated. Such extreme ranges of motion of smaller diameter surgical instruments within the cannula can create a “cat eye” or crescent shaped gap in the fixed seal that can result in a loss of seal integrity. Additional problems include the flexibility of the seal in maintaining its integrity when both small diameter and large diameter surgical instruments are used.
- Devices to restrict the diameter of a passageway in a trocar housing generally require an additional mechanism to be positioned on the proximal end of the trocar housing that restricts the range of motion of small surgical instruments. These diameter reducing devices, however, typically employ additional seals and/or structures that require adjustments by the user to accommodate different sized surgical instruments, thereby complicating the surgical process.
- A continuing need exists for a diameter reducing structure that can limit parallel off-axis as well as angular movements of small diameter surgical instruments and accommodate larger diameter surgical instruments without external adjustments.
- In accordance with a preferred embodiment, a surgical seal assembly includes a sleeve housing connected to a surgical sleeve, a seal housing including a seal member having inner portions adapted to permit passage of a surgical instrument in substantial sealed relation therewith, and a manual lock member movably mounted to the sleeve housing. The manual lock member is adapted for movement relative to the seal housing between a first position corresponding to a release position of the seal housing to permit detachment of the seal housing from the sleeve housing and a second position corresponding to a lock position of the seal housing to secure the seal housing to the sleeve housing. The manual lock member is preferably adapted for rotational movement relative to a longitudinal axis of the seal housing to move between the first and second positions thereof.
- The manual lock member may include an annular member having at least one locking surface adapted to engage at least one corresponding locking tab of the seal housing upon movement of the manual lock member to the second position. The annular member defines a central aperture for permitting passage of the object. Preferably, the annular member defines a plurality of mounting recesses adjacent the central aperture and the seal housing has a plurality of locking tabs corresponding to the mounting recesses. The mounting recesses are in general alignment with the locking tabs of the seal housing when in the first position of the manual lock member to receive the locking tabs. The mounting recesses are thereafter displaced from the locking tabs upon movement of the manual lock member to the second position thereof. The manual lock member may include a manual grip member depending radially outwardly relative to the longitudinal axis of the seal housing. The manual grip member is dimensioned and configured for engagement by the surgeon.
- The surgical seal assembly may include at least two stand-off elements mounted within the seal housing distal of the seal member. The stand-off elements are adapted for pivotal movement between an initial position and a pivoted position to permit passage of the surgical object. The stand-off elements may be normally biased to the initial position to restrict off-axis movement of the surgical object with respect to a longitudinal axis of the seal housing. The at least two stand-off elements are preferably operatively coupled such that movement of at least one of the stand-off elements between the initial and pivoted positions causes corresponding movement of the other stand-off: elements.
- The sleeve housing may be adapted for connection to a cannula housing of a cannula assembly.
- In another preferred embodiment, a surgical system includes a cannula assembly including a cannula housing and a cannula sleeve extending from the cannula housing. The cannula sleeve defines a longitudinal axis and has a longitudinal passageway to permit passage of a surgical instrument. The surgical system further includes a surgical seal assembly incorporating first and second seal subassemblies. The first seal subassembly includes a first housing having a seal member defining inner portions adapted to permit passage of a surgical object in substantial sealed relation therewith. The second seal subassembly includes a second housing adapted for mounting to the cannula housing. A manual lock member is adapted for movement between a first position corresponding to a release position of the first subassembly to permit removal of the first subassembly from mounting to the second subassembly, and a second position corresponding to a lock position of the first subassembly to secure the first subassembly to the second subassembly. Preferably, the second subassembly includes the manual lock member.
- The manual lock member may be adapted for rotational movement relative to the longitudinal axis to move between the first and second positions thereof. One of the first and second seal assemblies includes a locking latch and the other of the first and second seal subassemblies includes a corresponding locking surfaces. The locking latch and the locking surface cooperate to secure the first seal subassembly to the second seal subassembly upon movement of the manual lock member to the second position thereof. The other of the first and second seal subassemblies includes a locking recess dimensioned for receiving the locking latch when the manual lock member is in the first position whereby upon rotation of the manual lock member to the second position the locking latch cooperatively engages the locking surface. Preferably, the first seal subassembly includes the locking latch and the second seal subassembly includes the locking recess and the locking surface. The first seal subassembly preferably includes a plurality of locking latches and the second seal subassembly includes a plurality corresponding locking recesses for receiving the locking latches.
- The second subassembly may include a zero closure valve adapted to open to permit passage of the surgical instrument and to substantially close in the absence of the surgical instrument.
- A method for performing a surgical procedure is also disclosed. The method includes the steps of:
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- providing an access assembly including an access housing and an access sleeve operatively connected to the access housing;
- mounting a seal assembly to the access housing with the seal assembly including a seal housing and a seal member mounted relative to the seal housing, the seal member including inner portions adapted to form a substantial seal about a surgical object introduced therethrough; and
- securing the seal housing relative to the access housing by moving a manual lock member associated with the access housing to cause corresponding structure of the access housing and the seal housing to cooperatively engage in secured relation therewith.
- Preferred embodiments of the presently disclosed trocar diameter reduction structures for trocar are described herein with reference to the drawings, wherein:
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FIG. 1 is a perspective view of one preferred embodiment of a valve assembly and diameter reduction structure for trocars constructed in accordance with the present disclosure; -
FIG. 2 is an exploded perspective view of the valve assembly and diameter reduction structure ofFIG. 1 ; -
FIG. 3 is a close-up perspective view of a proximal end portion of the valve assembly and diameter reduction structure ofFIG. 1 ; -
FIG. 4 is a close-up perspective view of the valve assembly and diameter reduction structure ofFIG. 3 partially disassembled showing a diameter reduction structure positioned in a diameter reduction structure foundation element; -
FIG. 5 is a close-up perspective view of the valve assembly and diameter reduction structure ofFIG. 1 partially disassembled showing, a second seal; -
FIG. 6 is a close-up perspective view of a linking member in accordance with the disclosure ofFIG. 1 ; -
FIG. 7 is a close-up perspective view of a distal end portion of the diameter reduction structure foundation element in accordance with the disclosure ofFIG. 1 ; -
FIG. 8 is a close-up perspective view of a stand off in accordance with the disclosure ofFIG. 1 ; -
FIG. 9 is a cross-sectional view of the valve assembly and diameter reduction structure ofFIG. 1 along lines 9-9; -
FIG. 10 is a close-up of the cross-sectional view of the valve assembly and diameter reduction structure ofFIG. 9 ; -
FIG. 11 is an exploded view of the diameter reduction structure and the diameter reduction structure foundation element ofFIG. 4 ; -
FIG. 12 is a perspective view of the valve assembly and diameter reduction structure ofFIG. 1 being operationally employed with a large diameter surgical instrument passing through the valve assembly and diameter reduction structure and into a tissue portion of a patient; -
FIG. 13 is a close-up of the cross-sectional view ofFIG. 12 along lines 13-13 showing the repositioning of the diameter reduction structure for the large diameter surgical instrument; -
FIG. 14 is a close-up cross sectional view of the valve assembly and diameter reduction structure ofFIG. 10 showing a small diameter surgical instrument being positioned at least partially therein; -
FIG. 15 is the cross-sectional view ofFIG. 14 showing the diameter reduction structure controlling the angular movement of a small diameter surgical instrument positioned therein; -
FIG. 16A is a top view of a second embodiment of a valve and diameter reduction structure constructed in accordance with the present disclosure; -
FIG. 16B is a cross-sectional view ofFIG. 16A alonglines 16B-16B showing a representative movement of one stand off member of the diameter reduction structure; -
FIG. 16C is. a cross-sectional view ofFIG. 16A alonglines 16C-16C showing the diameter reduction structure in a first position; -
FIG. 17 is a perspective view of a proximal end of a third embodiment of a diameter reduction structure for trocar constructed in accordance with the present disclosure; -
FIG. 18A is across-sectional view of the trocar illustrating the diameter reduction structure ofFIG. 17 alongline 18A-18A; -
FIG. 18B is a cross-sectional view of the valve assembly and diameter reduction structure ofFIG. 18A alongline 18B-18B; -
FIG. 18C is a cross-sectional view of the valve assembly and diameter reduction structure ofFIG. 18A alongline 18C-18C; -
FIG. 19 is a cross-sectional side view of a fourth embodiment of the valve assembly and diameter reduction structure constructed in accordance with the present disclosure; -
FIG. 20A is an enlarged cross-sectional view of the second embodiment of the stand off configuration of the diameter reduction structure for trocar ofFIGS. 18A, 18B , and 18C; -
FIG. 20B is an enlarged cross-sectional view of the stand off configuration of the diameter reduction structure for trocar ofFIG. 19 ; -
FIG. 20C is partial cross-sectional perspective view of a fifth embodiment of a diameter reduction structure constructed in accordance with the present disclosure; -
FIG. 21 is a top view of a sixth embodiment of a valve assembly and diameter reduction structure for trocar having a movable diameter reduction. assembly constructed in accordance with the present disclosure; -
FIG. 22A is a cross-sectional view of the valve assembly and diameter reduction structure for trocar stand for trocar ofFIG. 21 along line 21A-21A; -
FIG. 22B is the cross-sectional view of the valve assembly and diameter reduction structure for trocar ofFIG. 22A with the stand off assembly in the second position; -
FIG. 22C is the cross-sectional view of the stand off configuration ofFIG. 22A with the stand off assembly in a third position; and -
FIG. 23 is a cross-sectional view of an alternate embodiment of the valve assembly and diameter reduction structure ofFIG. 22A ; -
FIG. 24 is a perspective view of another alternate embodiment of the seal assembly shown mounted to a cannula assembly in accordance with the principles of the present disclosure; -
FIG. 25 is a perspective view with parts separated of the seal assembly and cannula assembly in accordance with the embodiment ofFIG. 24 illustrating the components of the first and second seal subassemblies; -
FIG. 26 is a side cross-sectional view taken along the lines 26-26 ofFIG. 24 illustrating the seal assembly mounted to the cannula housing of the cannula assembly in accordance with the embodiment ofFIGS. 24-25 ; -
FIG. 27 is a perspective view illustrating mounting of the first seal subassembly to the second seal subassembly in accordance with the embodiment ofFIGS. 24-26 ; -
FIG. 28 is a view illustrating the mounting tabs of the first seal subassembly in accordance with the embodiment ofFIGS. 24-27 ; -
FIG. 29 is a view illustrating the mounting recesses of the second seal subassembly for receiving the mounting tabs of the first seal subassembly in accordance with the embodiment ofFIGS. 24-28 ; -
FIG. 30 is a view of the seal assembly illustrating the manual lock member in a first position corresponding to a release position in accordance with the embodiment ofFIGS. 24-29 ; and -
FIG. 31 is a view of the seal assembly illustrating the manual lock member in a second position corresponding to a locked position in accordance with the embodiment ofFIGS. 24-30 . - The present disclosure contemplates the introduction into a body of a patient a trocar adapted for receiving all types of surgical instruments including clip appliers, graspers, dissectors, retractors, staplers, laser fibers, endoscopes, as well as electrosurgical cutting, coagulating, and ablation devices, and the like. All such objects are referred to herein as “instruments”.
- Referring now in specific detail to the drawings in which like referenced numerals identify similar or identical elements throughout the several views, and initially to
FIG. 1 , a novel valve assembly and diameter reduction structure fortrocar 100 is shown constructed in accordance with a preferred embodiment of the present disclosure and intended to be used in combination with a conventional trocar assembly andcannula 50 defining apassageway 25 aligned with a central longitudinal axis-X.Passageway 25 defines a first operational area. - Valve assembly and
diameter reduction structure 100 includesdiameter reduction assembly 200 located adjacent a proximal end portion andvalve assembly 300 located adjacent a distal end portion. Thediameter reduction assembly 200 of the present disclosure, either alone or in combination withvalve assembly 300 provides a seal between a cavity formed in the patient and the outside atmosphere during and subsequent to insertion of an instrument throughcannula 50. Moreover, valve assembly anddiameter reduction structure 100 is capable of accommodating instruments of varying diameter, e.g. from ranges such as 5 mm to 12 mm, by providing a gas tight seal with each instrument during surgical procedures. The flexibility of the present valve assembly anddiameter reduction structure 100 to retain a fluid tight seal greatly facilitates endoscopic surgery where a variety of instruments having differing diameters are often needed during a single surgical procedure and off axis movements as well as small tool surgical angulation is employed. - Valve assembly and
diameter reduction structure 100 is preferably detachably mountable to aproximal end 54 ofcannula 50. During surgery, the surgeon can remove thediameter reduction assembly 200 fromvalve assembly 300 at any time during the surgical procedure and, similarly, mountdiameter reduction assembly 200 tovalve assembly 300 to reconfigure diameter reduction structure andvalve assembly 100. In addition, diameter andvalve assembly 100 may be readily adapted to be mounted to conventional cannulas of differing structures, material, and lengths. The ability ofdiameter reduction assembly 200 to detach fromvalve assembly 300 facilitates specimen removal throughcannula 50 and reduces the profile ofcannula 50 whendiameter reduction assembly 200 is not needed at a particular point of the surgical procedure. It is envisioned thatassembly 200 can also be configured to adapt to a variety of valve assemblies. - Referring now to
FIGS. 2-3 , one preferred embodiment of the novel valve assembly anddiameter reduction structure 100 of the present disclosure will be discussed in detail.Diameter reduction assembly 200 includes anend cap 110, afirst seal 125, diameter reduction structure housing orfirst housing 210, a first O-ring 225, adiameter reduction structure 240, and a diameter reductionstructure foundation element 280. Diameterreduction structure foundation 280 is connected withvalve assembly 300. Seal housing 30 is configured to be removably connected tocannula 50. -
End cap 110 is generally tubular in shape and includes adistal end portion 112 and aproximal end portion 114. An annular shapeddisc 116 defines ahole 115 aligned with the central longitudinal axis.End cap 110 is removably connected with diameterreduction structure housing 210. -
First seal 125 is sealingly positioned between a distal side of the annular shapeddisc 116 ofend cap 110 and a proximal end portion of diameterreduction structure housing 210.First seal 125 forms a first exterior seal ofassembly 100 and may be any conventional type of seal such as, but not limited to, a fixed or floating seal. - Diameter
reduction structure housing 210 has a generally hemispherical shell shape decreasing in circumference from adistal end portion 212 to aproximal end portion 214. Correspondingly,distal end portion 212 defines ahole 215 having a diameter larger than the diameter defined byannular portion 213 ofproximal end portion 214.Hole 215 is concentrically aligned with the central longitudinal axis-X.Proximal end portion 214 is configured to be connectively received bydistal end portion 112.Distal end 212 includes an outsidecylindrical portion 216 having a scalloped surface to facilitate handling thereof. A first O-ring 225 is seated on the inside surface of diameterreduction structure housing 210 in the vicinity ofannular portion 213. - Referring now to
FIGS. 2 and 4 , diameter reductionstructure foundation element 280 is configured to seatdiameter reduction structure 240 on itsproximal end portion 284 and support the movement of thediameter reduction structure 240 through a predefined range of motion and, in cooperation withhousing 210, provides a suitable support structure forstand offs 250 when limiting the operational diameter of thepassageway 25 through valve assembly anddiameter reduction structure 100.Foundation element 280 has an outsidecylindrical surface 286 and further defines a distally positioned generally tubular shapedportion 285 centered on the longitudinal axis. -
Diameter reduction structure 240 includes a stand off assembly 245 having three stand offmembers 250 interconnected by alinking mechanism 270 having three linkingmembers 271 in this one preferred embodiment.Stand offs 250 provide a predetermined degree of control over the movements of an instrument positioned withinassembly 100. Linkingmechanism 270 integrates and synchronizes the movement ofstand offs 250. - Each linking
member 271 is connected with and positioned between twoadjoining stand offs 250 such thatdiameter reduction structure 240 forms an approximately hexagonal configuration of alternatingstand offs 250 and linkingmembers 271 centered around longitudinal axis X. - Each stand off
member 250 includes acylindrical cogwheel portion 252 defining a longitudinal axis-Y (seeFIG. 8 ) and having opposingcylindrical end portions 254 with gears having cogs orteeth 255 extending parallel to longitudinal axis-Y. Linkingmembers 271 also have a cylindrical shape defining a longitudinal axis-Z (seeFIG. 6 ) and opposing ends 274 with gears having cogs orteeth 275.Teeth 275 extend parallel with the longitudinal axis-Z. Linkingmembers 271 and stand offmembers 250 are positioned in diameter reductionstructure foundation element 280 such that eachrespective cog beveled slot diameter reduction structure 240 to integrate and coordinate the simultaneous movement of each stand off 250. - Linking
members 271 provide a synchronizing function for the pivotal movement ofstand offs 250 throughout their range of movement, wherein thediameter reduction structure 240 is at least partially repositioned to accommodate a larger diameter surgical instrument. The limitations of movement of thediameter reduction structure 240 in the second position include factors such as the diameter of the cannula, shape of the stand off, and internal portions of the trocar that limit the pivotal or rotational type travel ofstand offs 250 away from the longitudinal axis. The second position is defined as when standoffs 250 are pivoted, flexed, or rotated in their seated position indiameter reduction structure 280 in a generally arcuate path distally and away from the longitudinal axis to increase thepassageway 25 diameter defined by the interrupted annular barrier ofdiameter reduction structure 240. - Diameter
reduction structure housing 210 and diameter reductionstructure foundation element 280 are configured to support the positioning, diameter control function, and movement ofdiameter reduction structure 240.Housing 210 andfoundation element 280 may be adapted to interface with a variety of different end caps, first seals, and seal housings, for example, as well as varying cannula sizes. - Referring now to
FIGS. 2 and 5 ,valve assembly 300 includes a second O-ring 335, a firstseal support member 350, asecond seal 365, a secondseal support member 380, a third O-ring 395, and a seal housing orsecond housing 310 configured for connecting to cannula 50. Diameterreduction structure foundation 280 provides seating for second O-ring 335 providing a seal betweendistal end 282 and aproximal end portion 354 of firstseal support element 350. - A
second seal 365 includes aflange 367 for being sealingly positioned between a distal end portion 352 of firstseal support element 350 and aproximal end portion 384 of secondseal support element 380. Firstseal support element 350 is generally annular in shape with an outsidecylindrical surface 356 and has three distally extendingtabs 358. A secondseal support element 380 also has a generally annular shape with an outside cylindrical surface 386 and is configured with radially extendingtabs 388. A third O-ring 395 provides a seal between secondseal support element 380 and sealhousing 310. -
Seal housing 310 has aproximal end portion 314 including radially alignedslots 318 configured to correspondingly mate withtabs 388 and adistal end portion 312 configured to mate withcannula 50 utilizing a suitable attachment mechanism such as a bayonet or threaded connection. -
Seal housing 310 further includes two diametrically opposedcantilevered portions 325. Each cantilevered portion includes twoopposed notches 326 havingsuture attachment fixtures 327 generally perpendicular toportions 325.Attachment fixtures 327 include acylindrical portion 328 and ahemispherical portion 329 configured for an easy tie off of sutures for the positive retention of the trocar assembly in position within the patient against the sufflation pressure typically employed in minimally invasive surgery. -
Second seal 365 is shown as a duck bill type seal, but it may be any seal system such as a frusto-conical seal, for example, that may be adapted to perform the function of a second seal. Secondseal support element 380 is positioned inseal housing 310. -
End cap 110, diameterreduction structure housing 210, diameter reductionstructure foundation element 280, firstseal support element 350, secondseal support element 380, and sealhousing 310 are preferably made of a medical grade plastic, metal, or composite materials having suitable strength and resilience for its application. In one preferred embodiment, the above assemblies are injection molded using a medical grade plastic. The O-rings are made of a medical grade plastic or rubber suitable for providing a fluid tight seal between generally rigid structural members. - Referring now to
FIGS. 6-8 , in one preferred embodiment, linkingmember 271 is shown aligned with longitudinal axis-Z. Aband 272 having an increased circumference and predetermined width is positioned on thecylindrical surface 274 of each linkingmechanism 270.Cogs 275 have a first arcuate width congruent at the outside surface ofcylindrical portion 274 that tapers or bevels to a narrower second arcuate width at the opposing side of eachcog 275. Thus, cogs 275 extend inwardly fromsurface 274 to a predetermined point betweensurface 274 and longitudinal axis-Z.Cogs 275 extend beyond and at least partially surround a recessedflat portion 278 that may include at least onepin 279.Pin 279 is concentric with longitudinal axis-Z and extends axially.Slots 277 are defined by cogs orteeth 275 and beveled portions ofcylindrical portion 274. - Diameter reduction
structure foundation element 280 is shown withdistal end portion 282 connecting with tubular shapedportion 285 andproximal end 284. Tubular shapedportion 285 is positioned to guide instruments being inserted into the second seal and has an inside diameter at least approximately equal to the diameter ofpassageway 25. Radially extendingtabs portion 285 andcylindrical portion 286, respectively, are configured and dimensioned to sealingly engage firstseal support element 350 withfoundation element 280 in combination with O-ring 335.Cylindrical portion 286 has an annular shape including aradially extending lip 281. Proximally extendingtabs 288 and at least partiallyconcave cavities 290 are configured to support the rotation or flexing ofdiameter reduction structure 240 withinproximal end portion 284. - Stand off
members 250 have ahead 260 connected by anarm 256 to abase portion 251 with opposingcylindrical end portions 254 aligned with a longitudinal axis-Y. Atubular band 252 has a circumference greater than the circumference ofend portion 254. A longitudinally alignednotch 252 a is formed inband 252 near the base ofarm 256.Cogs 255 have a first arcuate width congruent with the surface ofcylindrical portion 254 that tapers to a narrower second arcuate width at the opposing side of eachcog 255. Thus, cogs 255 extend inwardly fromsurface 254 to a predetermined point betweensurface 254 and longitudinal axis-Y.Slots 257 are defined by cogs orteeth 255 and beveled portion ofcylindrical end portion 254.Cogs 255 extend along axis-Y beyond and at least partially surround a recessedflat portion 258 that may include apin 259.Pin 259 is concentric with longitudinal axis-Y and extends axially fromportion 258.Head 260 has a generally hemispherical or bulbous shape having an exterior surface and a concaveinterior surface 266. -
Head 260 includes afirst side 262 having a generally planar face and an opposing taperedsecond side 268.First side 262 includes a cantileveredextension 261. Athird side 264 includes a generally convex portion and beveledside portions 265. Afourth side 266, opposing, thethird side 264, has a generally planar face that is connected witharm 256.Head 260 also includes a centrally positioned segmentedconcave notch 263 approximately perpendicular to longitudinal axis-Y. The generally concave shape ofnotch 263 is configured and dimensioned to accommodate a limited degree off axis movement by small surgical tools whendiameter reduction structure 240 is in a first or initial position.Arm 256 connectshead 260 withbase portion 251. -
Diameter reduction structure 240 components, including stand off assembly 245 andlinking mechanism 270,. are preferably fabricated from at. least one medical grade plastic, laminates of medical grade plastics, or composite materials of suitable flexibility, bias, rigidity, and compressive strength for application as diameter reduction structure. Different materials may also be bonded together in this structure depending on the application, for example,head 260 may be fabricated from one medical grade plastic that is of greater resiliency than a second medical grade plastic that formsarms 256. Similarly, linkingmembers 271 may be formed of similarly suitable one or more medical grade plastic or composite materials. - Further, the system of cogs synchronizing the movement of
stand offs 250 and linkingmembers 271 are but one type of linkingmechanism 270 known by those skilled in the art suitable for synchronizing the movements ofstand offs 250 and other suitable alternative mechanisms such as, but not limited to a pulley system, a flexible synchronizing shaft, or an articulated joint performing the same function are envisioned. - Referring now to
FIGS. 9 , and 10, valve assembly anddiameter reduction structure 100 andcannula 50 are shown in cross-section.First seal 125 includes concave orarcuate membrane portion 127 that extends radially inwardly and distally forming adistal end portion 128 defining ahole 129.Portions 127 are in close proximity to or abut stand offmembers 250. Stand offmembers 250 are shown in a first position having an orientation generally perpendicular to central longitudinal axis-X. The depth and width ofsegmented notches 263 are shown relative tohole 129 andsecond side 264 and provide a limited and increased degree of off axis movement or angular movement of small surgical instruments. -
Stand offs 250 include abase portion 251 positioned in proximity to or abutting cantileveredportion 218.Cantilevered portion 220 includeswall 222 configured to act as a stop to limit the radially outward movement ofheads 260 of stand offmembers 250. The material of construction of stand off members, and especiallyhead 260, may be selectively controlled to provide a range of flexibly compressive bias against parallel off axis and angular movements or surgical instruments. - Diameter
reduction structure housing 210 at least partially encloses diameter reductionstructure foundation element 280 and firstseal support element 350.Flange 367 ofsecond seal 365 is secured between firstseal support element 350 and secondseal support element 380.Seal housing 310 at least partially encloses secondseal support element 380.Cannula 50 connects withdistal end portion 312 ofseal housing 310. - In
FIG. 11 ,diameter reduction structure 240, shown as an integrated assembly in the first position, for placement within diameter reductionstructure foundation element 280.Foundation element 280 is configured to provide suitable positioning fordiameter reduction structure 240 to control the operable diameter and thus improving the ability of the sealing system ofassembly 100 to retain its integrity during procedures utilizing small instruments. This includes a suitable supporting structure forstand offs 250 to act as a barrier providing a controlled limitation to the movement of surgical instruments and supporting the movement ofdiameter reduction structure 240 between the first and second positions. - The first position of
structure 240 being defined by.heads 260 forming an interrupted annular barrier structure suitable for controlling forces in a plane generally orthogonal to the longitudinal axis-X resulting from parallel off axis and angular movements or movements generally orthogonal to the longitudinal axis of small surgical instruments positioned inpassageway 25. Thethird sides 264 ofheads 260 defining the second operable area in the first position. - In the first position, beveled
portions 265 ofheads 260 define gaps or interruptions in the annular barrier structure formed bydiameter reduction structure 240. The size of the gap is controlled by the shape and position ofheads 260 and is configured to ensure smaller diameter surgical instruments are precluded from passing betweenheads 260.Diameter reduction structure 240 further includes a controlled bias configured to resist the movement ofreduction structure 240 radially in an outward direction as well as from the first position to the second position. The bias instructure 240 also serves to returnstructure 240 to the first position after the removal of the larger diameter surgical instrument. - The second position being defined by
diameter reduction structure 240 moving at least partially distally to accommodate the unrestricted passage or of individual larger sized diameter surgical instruments throughdiameter reduction structure 240 andcannula 50. -
Foundation element 280 includes at least partiallyconcave seating positions 296 for linkingmembers members 250. Seatingpositions 290 define an interrupted channel having two distinct seats or supports 292 configured and dimensioned to receivecylindrical end portions 254.Band 252 is positioned between supports 292. Seatingpositions 290 further include anarcuate support member 294 with a proximally extendingstraight portion 299. - Seating
positions 296 define an at least partiallyconcave channel portions 298 separated by a slot orrecess 297 configured and dimensioned to receivesurface 274 andband 272 of linkingmember 271. Seatingpositions 296 include a proximally extendingstraight portion 299. - Seating
positions proximally extending member 295.Member 295 is connected by arms toportions portions - Seating
positions cogs respective slots stand offs 250 and linkingmembers 271. In addition,diameter reduction structure 240 includes a bias to the first position as individual components or as an assembly either as a result of its positioning within diameter reductionstructure foundation element 280, a separate bias member such as an elastic band, or by combinations thereof. When fully assembled with diameter reduction structure housing 210 (seeFIG. 2 ) and diameterreduction structure foundation 280,diameter reduction structure 240 is capable of performing its functions at any angle or in any direction of use without any operator action. - Referring now to
FIGS. 12 and 13 ,diameter reduction structure 100 is shown in an operational position. A large diametermedical instrument 80 defining a second longitudinal axis is positioned through valve assembly anddiameter reduction structure 100 andcannula 50. A large diameter surgical instrument is an instrument having a diameter or an cross-sectional area orthogonal to the second longitudinal axis less than a first diameter or first operable area ofpassageway 25, but greater than the second diameter or second operable orthogonal to the central longitudinal axis defined by the stand off assembly in the first position. Similarly, a small diametersurgical instrument 60 defining a first longitudinal axis has a diameter or cross-sectional area orthogonal to the first longitudinal axis less than the second diameter or second operable defined by the stand off assembly in the first position. Thus, the large instruments by definition being larger than the second operable area must at least partially deflect stand offassembly 240 distally in order to enter the passageway. In contrast, the small instruments can be positioned axially within the second operable area without deflecting stand offassembly 240. In this one preferred embodiment, large instruments are those defined as having diameters greater than 5.5 mm and small instruments those defining diameters equal to or less than 5.5 mm. The 5.5 mm distinction between large and small instruments is relative to the diameter of the passageway defined in the trocar and can vary depending upon the diameter of the trocar apparatus the valve assembly anddiameter reduction structure 100. Whenlarge diameter instrument 80 is moved distally along central longitudinal axis-X throughfirst seal 125 and into contact withdiameter reduction structure 240, the axially aligned force component movinglarge diameter instrument 80 has to overcome the bias configured to retaindiameter reduction structure 240 in the first position, as shown inFIG. 10 . - As the force behind
instrument 80 exceeds the bias configured to maintaindiameter reduction structure 240 in the first position,diameter reduction structure 240, pivots or rotates in a generally arcuate movement in a generally distal direction initially and then continues its pivotal or rotational arcuate movement, as shown by arrows “A” and “B”, away from the central longitudinal. axis to define the third operable area and accommodate the passage oflarge diameter instrument 80. The amount of bias employed to retaindiameter reduction structure 240 in the first position is controlled by factors such as the materials of construction of diameter reduction structure. 240 as well as the methods employed of securingdiameter reduction structure 240 in position in diameter reductionstructure foundation element 280. - When forced towards. the inside diameter of
wall 356 by the shaft of large diameter ofinstrument 80, standoffs 250 move to a second position whereinface 262 ofhead 260 is placed approximately parallel with and in apposition towall 356. The spatial relationship betweenwall 356 anddiameter reduction structure 240 in the second position is a function of individual trocar interior configurations, the inside circumference ofpassageway 25, and the intended application of the valve assembly anddiameter reduction structure 100. Valve assembly anddiameter reduction structure 100 is configured to provide suitable space for the pivoting or flexing ofdiameter reduction structure 240 and still accommodatelarger diameter instruments 80 that conform with the maximum inside diameter for a given.cannula 50. Upon withdrawal oflarger diameter instrument 80,diameter reduction structure 240 is biased to reposition to a first position wherein a portion of each stand off 250 isadjacent wall 220. - Referring now to
FIGS. 14 and 15 , stand offmembers 250 are shown in a first or diameter reduction position, whereinhead 260 extends in a generally radial direction relative to longitudinal axis-X.Cantilevered portion 222 provides a generally rigid barrier configured to structurally support and limit the radial displacement ofhead 260.Diameter reduction structure 240 in the first position is configured to accommodate the penetration ofsmaller diameter instruments 60 through valve assembly anddiameter reduction structure 100 and intocannula 50 without any movement. - When in this first position, stand off
member 250 is placed at least partially in axial compression by a force with a component perpendicular to central longitudinal axis-X as a result of the orthogonal or angular movements of a small diametersurgical instrument 60. Each stand offmember 250 is mounted indiameter reduction assembly 200 to provide a limit to excessive parallel off axis and angular movements of small diametersurgical instruments 60. - A small diameter
surgical instrument 60 is positioned throughseal 125 and intocannula 50 typically with little or no substantial contact withdiameter reduction structure 240. When small diametersurgical instruments 60 are manipulated to make off axis or angular movements, however, small diametersurgical instruments 60 come in contact with at least onehead portion 260 and the inside circumference ofcannula 50 which act in combination as two separate and approximately parallel structural barriers to control outwardly directed off axis and angular movements away from central longitudinal axis-X. The combination ofhead 260 and cantileveredportion 222 may be configured as a rigid or flexible biased structure. This controlling mechanism functions to bound the operational movements by small diametersurgical instruments 60, sufficiently to retain the integrity of the sealing system. - Referring now to
FIGS. 16A, 16B , and 16C, in another preferred embodiment, valve assembly anddiameter reduction structure 500 includes a proximal end portion or diameter reduction assembly 600 and a valve assembly 700 similar to the previous embodiment, however,diameter reduction structure 640 is positioned proximal to afirst seal 525. -
Diameter reduction structure 500 includes anend cap 510, a diameterreduction structure housing 610, adiameter reduction structure 640, a diameter reductionstructure foundation element 680, and as required a first O-ring. -
End cap 510 has a generally cylindrical shape including adistal end portion 512 and aproximal end portion 514.Proximal end portion 514 includes an annular shaped disc orportion 516 defining ahole 515 aligned with the central longitudinal axis-X. In this configuration,annular portion 516 may be a rigid plastic or a flexible membrane not configured to be a seal. Thus,hole 515 could be configured as a rigid or flexible barrier and having a diameter at least equal to the. inside diameter of acannula 50 in a rigid configuration. - Diameter
reduction structure housing 610 has a generally hemispherical shell shape decreasing in circumference from adistal end portion 612 to aproximal end portion 614.Proximal end portion 614 includes anannular portion 613 defininghole 615.Hole 615 preferably has a larger diameter thanhole 515.Proximal end portion 614 is configured to be connectively received bydistal end portion 512.Distal end portion 612 includes an outsidecylindrical portion 616 having a scalloped surface to facilitate handling thereof. -
Diameter reduction structure 640 includes a stand off assembly having three stand offmembers 650 and alinking mechanism 670 is positioned proximal to afirst seal 525.Stand offs 650 provide a predetermined degree of control over and limitation to the movements of instruments positioned within assembly 600. Linkingmechanism 670, in the form of three linking members 671, integrate and synchronize the movement ofstand offs 650. While the specific configuration of stand offmembers 650 or linkingmechanism 670 may vary, stand off assembly 645 is employed operationally as described in all of the embodiments herein to limit the off-axis and angular movements of small surgical instruments. - Diameter reduction
structure foundation element 680 is configured to seatdiameter reduction structure 640 on. its proximal end portion 682 and includes at least partially cantilevered seatingpositions 690 configured to support and control the movement ofreduction structure 640 throughout a predefined range of motion as at least partially represented by arrow “A”. A distally extendingtubular portion 685 is configured for the positioning offirst seal 525.First seal 525 is positioned approximately orthogonal to longitudinal axis-X and may be a fixed or- a floating type seal. - A first seal support element 750 has a generally tubular shape with a
distal end portion 754 abutting a proximal side ofcantilevered seating portion 690 and adistal end 752. First support element 750 has aninside wall 756 that may be configured to limit the distal range of motion ofstand offs 650. A cantileveredportion 753 of first seal element 750 is positioned to secure and seal aflange 767 of asecond seal 765 in positioned between a proximal portion of secondseal support element 780. - A
distal end 752 of first support element 750 at least partially encloses and sealingly positions aflange 767 ofsecond seal 765 in cooperation with adistal end portion 782 of a secondseal support element 780.Second seal 765 may be any type of seal, but is preferably a duck bill type seal commonly configured for use with a fixed or floating first seal. In the preferred embodiment,second seal 765 is a duck bill type seal extending distally into aseal housing 710. -
Seal housing 710 includes aproximal portion 714 configured to secure and at least partially enclosesecond seal 765 and at least a portion of secondseal support element 780 and first seal support element 750. Secondseal support element 780 also has a generally annular shape and is configured to lock with and engage first seal support element 750.Seal housing 710 has adistal end portion 712 configured to mate with a cannula. - Valve assembly and
diameter reduction structure 500 is configured as an assembly for controlling the off axis and angular movements of small surgical instruments externally or proximally to the sealing system. This configuration reduces the strain placed on the first seal by further limiting the range of angular motion to which the first seal is subjected to by small surgical instrument manipulation and thereby improving the integrity of the trocar sealing system. In addition, while valve assembly anddiameter reduction structure 500 may be removably connected to a correspondingly dimensionedcannula 50, it is also envisioned thatend cap 510,housing 610,diameter reduction structure 640, andfoundation element 680 may be readily adapted as an integrated assembly, for example, with or without an integratedfirst seal 525, for use with a wide range of trocar assemblies having fixed or floating seals to advantageously control off-axis and angular movements of small surgical instruments without interrupting the integrity of the sealed portions of the trocar. - Referring now to
FIGS. 17 and 18 A-18C, one of the preferred embodiments of a valve assembly anddiameter reduction structure 800 includes a proximal end portion ordiameter reduction assembly 900 and a distal end portion orvalve assembly 1000.Diameter reduction structure 940 is positioned distal to afirst seal 825 and within a diameterreduction structure housing 910. -
Diameter reduction structure 940 is illustrated with a stand off assembly. 945 having threestand offs 950 and three linkingmembers 971 positioned in a diameter reduction structure foundation 980.—While the general configuration of diameterreduction structure foundation 980 and linkingmembers 971 are structurally and operationally similar to earlier embodiments, standoffs 950 have a differentconfiguration head portion 960, similar to that depicted inFIG. 16A , withside portion 965 having a generally planar shape and a width approximately equivalent toarm 956. -
Head portion 960 may also include anattachment mechanism 963 and a cantilevered extension orflange 967.Flange 967 extends radially fromhead 960 toward base 961 in the first position. In the second position of stand off 950,flange 967 can be configured with a suitable length to at least partially limit the range of movement of stand off 950 by contacting an inside wall of diameterreduction structure housing 910.Attachment mechanism 963 is configured to receive and retain an annularly shapedbias member 969 on stand off 950 throughout its range of motion. Annularly shaped biasedmember 969 is configured to biasstand offs 950 to the first position, provide an additional bias when off axis or angular movements act to. compress a stand off 950 in a radially outward direction against the. diameterreduction structure foundation 980 orhousing 910, and act as an uninterrupted barrier to preclude smaller diameter surgical instruments from intruding betweenstandoffs 950. - The combined effect of
attachment mechanism 963,flange portion 967, andbias member 969 is the control by stand offassembly 940 of the movement of smaller diameter surgical instruments when forces having a generally orthogonal orientation to the longitudinal axis are employed as well as the ability of stand offassembly 940 to automatically accommodate larger diameter instruments. - In
FIG. 19 , an additional preferred embodiment of valve assembly anddiameter reduction structure 1200 is configured with adiameter reduction structure 1340 including a stand offassembly 1345 having four diametrically opposedstand offs 1350 independently positioned within a diameter reduction structure foundation. 1380. Each stand off 1350 independently pivots, without a linking mechanism, to limit off-axis and angular movements of small instruments. - Stand off
members 1350 include ahead 1360, anarm 1356, and abase element 1351 configured for mounting withfoundation 1380. Stand off 1350 can be fixedly mounted to foundation 1380 j or example, or in thealternative base element 1351 may be pivotally positioned onfoundation 1380 and retained in place using a positioning element (not shown). A bias is employed to position stand off 1380 to a first position adjacent housing 1310. As a further alternative embodiment, a linking mechanism may be positioned to be operative withheads 1360 to perform, for example, one or both functions of the linking mechanism shown previously.Alternative head 1360 configurations include having telescoping, tongue and grooved, or beveled gear mechanisms that interrelatestand offs 1380 into an approximately contiguous annular structure throughout their range of motion. - A bias inherent in stand off 1350 or in combination with its positioning element to the diameter
reduction structure foundation 1380 maintainsstand offs 1350 in the first position unless deflected by a large diameter surgical instrument. As shown in other embodiments,diameter reduction structure 1350 may be employed proximal to or distal to a first seal.Stand offs 1350, in this configuration, also include a bulbous shapedhead 1360, similar to that ofhead 260 for controlling the movements of smaller diameter surgical instruments. - In
FIGS. 20A and 20B , two embodiments of stand offmembers FIGS. 18A-18C and 19, respectively. These two major configurations of stand offs, however, are only to be considered to be representative of all the stand off configurations described herein. Stand offmembers base portions Heads stand offs - All the stand offs described herein provide a generally compression resistant biased structure against forces acting in a plane having a generally orthogonal orientation to the “X” or central longitudinal axis. It is envisioned that stand
offs - Individual stand off
members head portion adjacent stand offs retention mechanism 939 can also be included inhead portion biased member 939. - Referring now to
FIG. 20C , in a further alternate embodiment of adiameter reduction structure 1440, a single unified stand off assembly 1445 is formed into a continuous and integrated flanged stand off or flange structure 1445. Flange structure 1445 may take any configuration ofhead 1460,arm 1456, andbase 1451, for example, suitable for performing the function of limiting the movement of smaller diameter surgical instruments when moved generally parallel off-axis or angularly.Diameter reduction structure 1440 may be at least partially segmented with a plurality ofslots 1431 defining segmentedhead portions 1460 andarms 1456. Aretention mechanism 1439 can also be employed to further biasdiameter reduction structure 1440. This embodiment could also take the structural form of a cantilevered generally linear flexible flange structure or an angled stand off structure at least partially cantilevered and supported by a correspondingly positioned structure housing. -
Diameter reduction structure 1440, withindependent stand offs 1450 or configured as an integrated unified flange structure stand off 1450, is suitably configured to resist forces in a plane transverse to central longitudinal axis “X” and in particular forces in a plane approximately orthogonal to the central longitudinal axis “X”.Flange structure 1450 is configured to flex or pivot with forces generally aligned with the longitudinal axis “X” so as to accommodate large diameter surgical instruments without any operational adjustments. - In another alternate embodiment the diameter reduction structure is a unified structure wherein the arms are joined to form an annular type structure configuration and are positioned within the trocar housing as an assembly. The stand off assembly in this embodiment can also include separate or integral biased members.
- In still another embodiment, one or more diameter reduction structures could be employed together in series or in one assembly to create parallel diameter reduction structures or diameter reduction structures of different diameters.
- Referring now to
FIGS. 21 and 22 A, a further alternate embodiment of a valve assembly anddiameter reduction structure 1500 includes adiameter reduction assembly 1600 andvalve assembly 1700. Valve assembly anddiameter reduction structure 1500 defines apassageway 1505 concentric with a central longitudinal axis-X. -
Diameter reduction assembly 1600 includes afirst seal 1525, diameter reduction structure housing ordistal housing 1610, adiameter reduction structure 1640, and a diameter reductionstructure foundation element 1680. Diameterreduction structure foundation 1680 connects withvalve assembly 1700. Seal housing orproximal housing 1710 ofvalve assembly 1700 is configured to be removably connected tocannula 50. - Diameter
reduction structure housing 1610 is generally tubular in shape and includes atubular wall 1615 defining adistal end portion 1612 and aproximal end portion 1614.Proximal end portion 1614 has aproximally extending rim 1616 defining a recessed portion orflange 1618.Flange 1618 is approximately perpendicular to the longitudinal axis-X and includes arim 1619 defining a hole orpassageway 1505 aligned with longitudinal axis-X. Diameterreduction structure housing 1610 in this configuration includes a first seal 1515 positioned distal toflange 1618 that is held in position by a firstseal support element 1620. Firstseal support element 1620 also defines arim 1622 aligned withrim 1619. A distal end ofrim 1622 forms anedge 1623 with adistal end 1622 ofseal support element 1620.Distal end portion 1612 includes aflanged portion 1613. - The inside diameter of
tubular wall 1615 abuts and is configured to slidingly move in relation to afirst member 1630 and a secondannular member 1635. Adistal edge 1631 ofannular member 1630 is positioned abutting aproximal edge 1636 of secondannular member 1635. Secondannular member 1635 has a radially extending protuberance ortab 1637. -
Diameter reduction housing 1610 is connected to anannular member 1611 extending distally fromdistal end 1612. Astop 1608 is positioned on adistal end 1609 ofmember 1611 that abuts aseal support element 1750 and defines a first position ofhousing 1610.Stop 1608 also interfaces with and is limited bytab 1637 to at least partially limit the proximal travel ofhousing 1610 and defines a second position ofhousing 1610. -
Diameter reduction structure 1640 is positioned on a diameterreduction foundation element 1680. Diameterreduction foundation element 1680 has adistal end 1682 and a proximal end 1684.Distal end 1682 abuts withseal support element 1750.Element 1680 also abuts with a portion of the inside ofannular members Diameter reduction structure 1640 is configured to support up to approximately 180° of travel of each stand offmember 1650 from a position extending distally approximately parallel to the longitudinal axis to a position extending proximately approximately parallel to the longitudinal axis. - In a first stand off
assembly 240 position, stand offmembers 250 are generally positioned in a plane orthogonal the central longitudinal axis and to reduce the operable area ofpassageway 1505 in. combination with the structural support ofhousing 1610. In a second stand offassembly 240 position, stand offmembers 250 are generally positioned at least partially distal to the first position. In a third stand. offassembly 240 position, stand offmembers 250 are generally positioned at least partially proximal to the first position. - Stand off
members 1650 have ahead 1660 connected by anarm 1656 to abase portion 1651 with opposing cylindrical end portions 1654. Stand offmembers 250 are connected by a linking mechanism including three linkingmembers 1671 as described in earlier embodiments. -
Head 1660 includes afirst side 1662 having a generally planar face and an opposing taperedsecond side 1668 in apposition withfirst seal 1525 whendiameter reduction structure 1640 is in the first position.First side 1662 includes a cantileveredextension 1661. Athird side 1664 includes a generally convex portion and beveledside portions 1665. Afourth side 1666, opposing, the third side, has a generally planar face that is connected witharm 1656 such that the planar face extends tosecond side 1662 and to cantileveredportion 1661.Arm 1656 is a neck downportion connecting base 1651 andhead 1660.Head 1660 also includes a centrally positioned segmentedconcave notch 1663 approximately perpendicular to longitudinal axis-Y. The generally concave shape ofnotch 1663 is configured and dimensioned to accommodate a limited degree off axis movement by small surgical tools whendiameter reduction structure 1640 is in a first or initial position. - While
diameter reduction structure 1640 is illustrated with stand off assembly 1645 having threestand offs 1650. and linking mechanism 1670 having three linkingmembers 1671, the general configuration of diameterreduction structure foundation 1680 and linkingmembers 1671 are structurally and operationally similar to earlier embodiments such as those. ofFIGS. 6-8 . -
Valve assembly 1700 includes a firstseal support member 1,750, asecond seal 1765, and aseal housing 1710 configured for connecting to cannula 50. In addition, an elastic tubular seal orthird seal 1601 is sealingly positioned over a sliding joint 1699 betweenvalve assembly 1700 anddiameter reduction assembly 1600. - Second
seal support element 1750 is positioned between diameterreduction foundation element 1680 and sealhousing 1710. Secondseal support element 1750 has a generally annular in shape with a tubular wall 1755 having an outside cylindrical surface 1756. In addition, a distal end 1752 of secondseal support element 1750 sealssecond seal 1765 in position in combination with a proximal end 1714 ofseal housing 1710. -
Seal housing 1710 proximal end portion 1714 includes positions for the seating of the secondseal support element 1750 andsecond seal 1765. Adistal end portion 1712 ofseal housing 1710 is configured to mate withcannula 50 utilizing a suitable attachment mechanism such as a bayonet or threaded connection. - Third or
tubular seal 1601 has aproximal end 1605 and adistal end 1603. Proximal end 1715 is sealingly engaged withflange 1613 ofdiameter reduction housing 1610. Proximal end 1714 ofseal housing 1710 and distal end 1752 of secondseal support element 1750 are positioned to sealingly engage adistal end portion 1603 ofthird seal 1601.Third seal 1601 is configured and dimensioned as a flexible elastic tubular seal positioned over and providing a seal for sliding joint 1699.Third seal 1601 is suitably flexible for accommodating the movement ofdiameter reduction housing 1610 between the first position whereinstop 1608 is abutting secondseal support element 1750 and the second position whereinstop 1608 is repositioned proximally and is abuttingtab 1637. In addition,third seal 1601 provides a bias to the first position ofdiameter reduction housing 1610 ofseal housing 1610. -
Third seal 1601 is preferably fabricated from a flexible and/or stretchable material preferably an extrudable or injected moldable material, most preferably an elastomer or elastomeric or elastomer material.Third seal 1601 may include acentral shape indentation 1601 a to permit longitudinal extension and retraction ofstructure housing 1610. Alternatively, third seal may be completely tubular devoid of v-shape indentation as depicted inFIG. 23 , and have suitable elastomeric properties to permit the seal to stretch during extension and retraction of thehousing 1610. An elastomer material having a suitable thickness for external instrument applications that can encounter rugged handling and is resistant to tearing or penetration, for example, while providing a flexible bias. It is also envisioned thatthird seal 1601 can be readily attached and detached, as required, for autoclaving or sterilization. - Referring now to
FIGS. 22A-22C ,diameter reduction structure 1640 is biased to a first position, similar to that ofFIGS. 15, 16A , and 20A wherein at least a portion offourth side 1666 ofhead 1660 andarm 1656 are in apposition with a portion of diameterreduction structure housing 1610 and stop 1608 is abutting secondseal support element 1750. In this embodiment, rim 1621 anddistal end 1622 of firstseal support element 1620 are in apposition with at least a portion offourth side 1666 andarm 1656, respectively and in particular,corner 1623 is positioned at the junction ofarms 1656 and sidefourth side 1666. Thus, firstseal support element 1620 supports standoffs 1650 in the first position by providing structural support forstand offs 1650 to limit from the off axis and angular movements of small diameter surgical instruments. - When
diameter reduction structure 1640 is deflected distally by a large surgical instrument, such as shown in.FIG. 13 , to the second position whereinface 1662 is pivoted in the direction of the inside of tubular wall 1755 of secondseal support element 1750, stand offmembers 1650 are accommodating the increased diameter of the large surgical instrument without any external adjustments by the surgeon or operator. Stand offmembers 1640, however; retain their bias to the first position. - When the large surgical instrument is withdrawn proximally through valve assembly and
diameter reduction structure 1500, the combination of the bias and elastic nature of stand offmembers 1650 may bind with the large instrument. To preclude undesirable binding,distal end 1612 is slidingly engaged with firstannular member 1630, secondannular member 1635, and secondseal support element 1750 such that thediameter reduction housing 1610 slides proximally until the instrument ceases to bind or stop 1608abuts tab 1637. The proximal movement ofdiameter reduction structure 1610 from thefirst housing 1610 position defines an increased volume withindiameter housing 1610 that is suitable for stand offmembers 1650 to pivot proximally to the third position and at least partially increase the operable area ofpassageway 1505 from the second operable area to a third operable at least wherein the operable area is increased similar to that of the second position of the stand off assembly such that the large instrument can be withdrawn with limited resistance. - Additional alternative embodiments for precluding binding include a catch or an engaging receptacle for each stand off in the second position with an external release mechanism, for example, or a friction reducing means such as one or more wheels positioned on
second side 1668 and/orthird side 1664 that could accommodate the withdrawal of the large instrument while in a distal or second position by the rotation of the wheel and still provide adequate resistance to movements of small surgical instruments when in the first position. - Referring now to
FIG. 24 , there is illustrated another embodiment of the present disclosure.System 2000 includesseal assembly 2002 andcannula assembly 2004 to which theseal assembly 2002 is mounted.Seal assembly 2002 defines a seal housing consisting of a plurality of components forming an outer member of theseal assembly 2002, and diameter reduction structure for limiting excessive off-axis and angular movements of small diameter surgical instruments as discussed hereinabove.Seal assembly 2002 defines seal axis “x”.Seal assembly 2002 includes first orproximal seal subassembly 2006 and second ordistal seal subassembly 2008 which is connected tocannula assembly 2004.First seal subassembly 2006 is adapted for releasable connection tosecond seal subassembly 2008 and incorporates the diameter reduction structure. - With reference now to
FIG. 25-27 , in conjunction withFIG. 24 , first andsecond seal subassemblies seal assembly 2002 will be discussed.First seal subassembly 2006 includesend cap 2010,septum seal 2012 anddiameter reduction housing 2014.Diameter reduction housing 2014 includes first and secondreduction housing components off elements 2020. In general, stand-off elements 2020 are interconnected and pivot to permit passage of an instrument. Stand-offelements 2020 are biased to an initial position by elastomeric O-ring 2022. O-ring 2022 is received withinrecess 2020 r of each stand-off element 2020 as shown inFIG. 26 . When stand-off elements 2020 pivot downwardly (shown in phantom inFIG. 26 ) upon insertion of an instrument, O-ring 2022 stretches to permit this movement of the stand-off elements 2020. Upon removal of the instrument, the stand-off elements 2020 return to their initial position in transverse relation to the axis “x” under the influence of the O-ring 2022. The remaining components offirst seal subassembly 2006 are substantially similar to their corresponding components disclosed and discussed in the prior embodiments, and reference is made hereinabove for a further discussion of the structure and functionality of these components. - In one further aspect of the present embodiment,
diameter reduction housing 2014 includes mountingtabs 2024 radially spaced aboutinterior wall 2026 of secondreduction housing component 2018. As seen inFIG. 25 andFIG. 27 , mountingtabs 2024 serve to releasably securefirst seal subassembly 2006 tosecond seal subassembly 2008 as will be discussed. -
Second seal subassembly 2008 includesstationary ring member 2028,duckbill valve housing 2030, zero closure orduck bill valve 2032 supported within thevalve housing 2030, andmanual lock member 2034.Stationary ring member 2028 defines firstannular wall 2036 on its proximal side.Annular wall 2036 incorporates small andlarge recesses annual wall 2036 ofstationary ring member 2028 is received withinannular gap 2042 defined betweenwalls reduction housing components FIG. 26 ). Small andlarge recesses positioning legs reduction housing 2014. As best depicted inFIGS. 28 and 29 , the respective distances between the positioninglegs recesses 2038, 2040 (identified as distances and lengths “a” and “b”) ensure proper orientation ofreduction housing 2014 within, or relative to,stationary ring member 2028 during assembly. -
Stationary ring member 2028 further includes secondannular wall 2052 disposed on the distal side of thestationary ring member 2028. Secondannular wall 2052 includes partialannular slot 2054 therein and a plurality of radially spacedgrooves 2056 in its outer surface. Asingle locking tab 2058 is disposed within eachgroove 2056. The functioning ofpartial slot 2054, spacedgrooves 2056 and lockingtabs 2058 will be discussed in greater detail hereinbelow. - As best depicted in
FIGS. 25 and 29 , duckbill valve housing 2030 includesannular wall 2060 which definescentral aperture 2062.Annular wall 2060 defines threegrooves 2064proximal aperture 2062.Grooves 2064 accommodate mountingtabs 2024 ofdiameter reduction housing 2014 during assembly of first andsecond seal subassemblies Duck bill housing 2030 includes a plurality of axial dependinglegs 2066.Legs 2066 of duckbill valve housing 2030 may includerectangular openings 2068. - In one preferred arrangement,
manual lock member 2034 is secured toduck bill housing 2030 in fixed relation therewith.Manual lock member 2034 includes a plurality ofrecesses 2070 defined in its outer surface.Recesses 2070 receive corresponding dependinglegs 2066 ofduck bill housing 2030.Recesses 2070 each include mounting tabs 2072 (as seen inFIG. 25 ) which are received withinrectangular openings 2068 of dependinglegs 2066 ofduck bill housing 2030 in snap relation therewith to secure the two components (see alsoFIG. 26 ).Manual lock member 2034 andduck bill housing 2030 capture theperipheral rim 2074 ofduck bill valve 2032 to secure theduck bill valve 2032 between the two components. -
Manual lock member 2034 andduck bill housing 2030 are at least partially disposed withinstationary ring member 2028 and are adapted for rotational movement relative to thestationary ring member 2028.Manual lock member 2034 includesgrip 2076 which extends radially outwardly for engagement by the user.Grip 2076 includestransverse leg 2078 which is accommodated within partialannular slot 2054 ofstationary ring member 2028 and traverses theslot 2054 during rotation ofmanual lock member 2034 andduck bill housing 2030.Manual lock member 2034 is adapted for rotational movement between a first position corresponding to a release position which permits mounting and/or release offirst subassembly 2006 fromsecond subassembly 2008, and a second position corresponding to a lock position which securesfirst subassembly 2006 to thesecond subassembly 2008. An O-ring seal 2080 may be positioned about the circumference ofduck bill housing 2030 to form a substantial seal between theduck bill housing 2030 anddiameter reduction housing 2014. - In other embodiments, the
manual lock member 2034 is slidably received byduck bill housing 2030. Themanual lock member 2034 is then slidable with respect tostationary ring member 2028. - With reference to
FIGS. 24-26 ,cannula assembly 2004 includescannula housing 2082 andcannula sleeve 2084 extending from thehousing 2082.Cannula housing 2082 includesvertical legs 2086 which are positioned withingrooves 2056 ofstationary ring member 2028.Legs 2086 preferably includeinternal ledges 2088 advantageously dimensioned to accommodate lockingtabs 2058 disposed within thegrooves 2056 ofstationary ring member 2028 to fixedly secure the two components.Cannula sleeve 2084 defineslongitudinal passage 2090 which permits passage of instrumentation.Cannula sleeve 2084 may be secured tocannula housing 2082 by correspondingtongues 2092 andgrooves 2094 of thecannula sleeve 2084 and thecannula housing 2082 respectively. An O-ring seal 2096 may be positioned withincannula housing 2082 for forming a seal within thehousing 2082 adjacent these components. - In use,
second seal subassembly 2008 ofseal assembly 2002 is mounted tocannula housing 2082. In this regard,vertical legs 2086 ofcannula housing 2082 are aligned withgrooves 2056 ofstationary ring member 2028 and thering member 2028 is advanced whereby thelocking tabs 2058 of thering member 2028 securely engage theinternal ledges 2088 within thevertical legs 2086. Thereafter, when it is determined that the diameter reduction structure is needed, for example, in use with a small diameter instrument,first seal subassembly 2006 is positioned relative tosecond seal subassembly 2008 as depicted inFIGS. 27-29 . In this position, positioninglegs first seal subassembly 2006 are aligned with the correspondingrecesses FIGS. 25 and 27 ). In addition,manual lock member 2034 is placed in the first or release position ofFIG. 29 . In this position, mountingtabs 2024 of thefirst seal subassembly 2006 are in general alignment with mountingrecesses 2064 of theannular plate 2060 ofduck bill housing 2030 of thesecond seal subassembly 2008.First seal subassembly 2006 is then mounted tosecond seal subassembly 2008 whereby positioninglegs respective recesses tabs 2024 are received within mountinggrooves 2064 ofduck bill housing 2030.Manual lock member 2034 is then rotated about axis “a” from the first or release position depicted inFIG. 30 to the second or lock position depicted inFIG. 31 . This movement ofmanual lock member 2034 causes corresponding rotational movement ofduck bill housing 2030 to displace the mountinggrooves 2064 whereby mountingtabs 2024 are captured beneathannular wall 2060 ofduck bill housing 2030. In this position,first seal subassembly 2006 is secured tosecond seal subassembly 2008. The procedure is continued by introducing an instrument through theseal assembly 2002 andcannula assembly 2004, and performing the desired surgical procedure. - It is noted that
duck bill housing 2030 andmanual lock member 2034 may be a single component monolithically formed during manufacture. In addition, it is envisioned that thesecond seal subassembly 2008 may be a component of the cannula housing orsleeve housing 2082, and supplied with thecannula assembly 2004. In the alternative,second seal subassembly 2008 may replace thecannula housing 2082 in its entirety and serve as the sleeve housing. It is further envisioned that other modified first seal subassemblies, for example, with or without diameter reduction structure, may be adapted for use with thesecond seal subassembly 2008. - Although the illustrative embodiments of the present disclosure have been described herein with reference to the accompanying drawings, it is to be understood that the disclosure is not limited to those precise embodiments and that various other changes and modifications may be affected therein by one skilled in the art without departing from the scope or spirit from the disclosure. All such changes and modifications are intended to be included within the scope of the appended claims.
Claims (19)
1. A surgical seal assembly, which comprises:
a sleeve housing connected to a surgical sleeve;
a seal housing including a seal member, the seal member having inner portions adapted to permit passage of a surgical instrument in substantial sealed relation therewith; and
a manual lock member movably mounted relative to the sleeve housing, the manual lock member being movable between a first position corresponding to a release position to permit detachment of the seal housing from the sleeve housing, and a second position corresponding to a lock position of the seal housing, to secure the seal housing to the sleeve housing.
2. The surgical seal assembly according to claim 1 wherein the manual lock member is adapted for rotational movement relative to a longitudinal axis of the seal housing.
3. The surgical seal assembly according to claim 2 wherein the manual lock member includes an annular member associated therewith, the annular member including at least one locking surface adapted to engage a corresponding at least one locking tab of the seal housing upon movement of the manual lock member to the second position.
4. The surgical seal assembly according to claim 3 wherein the annular member defines a central aperture for passage of the surgical object.
5. The surgical seal assembly according to claim 4 wherein the annular member defines a plurality of mounting recesses adjacent the central aperture, and the seal housing has a plurality of locking tabs corresponding to the mounting recesses, the mounting recesses in general alignment with the locking tabs of the seal housing when in the first position of the manual lock member to receive the locking tabs, the mounting recesses being displaced from the locking tabs upon movement of the manual lock member to the second position thereof.
6. The surgical seal assembly according to claim 5 wherein the manual lock member includes a manual grip member depending radially outwardly relative to the longitudinal axis of the seal housing, the manual grip member dimensioned and configured for engagement by the surgeon.
7. The surgical seal assembly according to claim 1 including at least two stand-off elements mounted within the seal housing distal of the seal member, the stand-off elements adapted for pivotal movement between an initial position and a pivoted position to permit passage of the surgical object, the stand-off elements being normally biased to the initial position to urge the surgical object into general alignment with respect to a longitudinal axis of the seal housing.
8. The surgical seal assembly according to claim 7 wherein the at least two stand-off elements are operatively coupled such that movement of at least one of the stand-off elements between the initial and pivoted positions causes corresponding movement of the other entering element.
9. The surgical seal assembly according to claim 1 wherein the sleeve housing is connected to a cannula assembly.
10. The surgical seal assembly according to claim 1 wherein one of the seal housing and the sleeve housing includes a locking tab and the other of the seal housing and the sleeve housing includes a locking access, the locking tab and the locking recess cooperating to secure the seal housing to the sleeve housing upon movement of the manual lock member to the second position.
11. A surgical system, which comprises:
a cannula assembly including a cannula housing and a cannula sleeve extending from the cannula housing, the cannula sleeve defining a longitudinal axis and having a longitudinal passageway to permit passage of a surgical instrument; and
a surgical seal assembly including:
a first seal subassembly including a first housing having a seal member defining inner portions adapted to permit passage of a surgical object in substantial sealed relation therewith;
a second seal subassembly including a second housing adapted for mounting to the cannula housing; and
a manual lock member adapted for movement between a first position corresponding to a release position of the first seal subassembly to permit release of the first seal subassembly from mounting to the second seal subassembly and a second position corresponding to a lock position of the first seal subassembly, to secure the first seal subassembly to the second seal subassembly.
12. The surgical system according to claim 11 wherein the second seal subassembly includes the manual lock member.
13. The surgical system according to claim 11 wherein the manual lock member is adapted for rotational movement relative to the longitudinal axis to move between the first and second positions thereof.
14. The surgical system according to claim 11 wherein the second subassembly includes a zero closure valve adapted to open to permit passage of the surgical instrument and to substantially close in the absence of the surgical instrument.
15. The surgical system according to claim 14 wherein one of the first and second seal assemblies includes a locking latch and the other of the first and second seal subassemblies includes a corresponding locking surface, the locking latch and the locking surface cooperating to secure the first seal subassembly to the second seal subassembly upon movement of the manual lock member to the second position thereof.
16. The surgical system according to claim 15 wherein the other of the first and second seal subassemblies includes a locking recess dimensioned for receiving the locking latch when the manual lock member is in the first position whereby upon rotation of the manual lock member to the second position the locking latch cooperatively engages the locking surface.
17. The surgical system according to claim 16 wherein the first seal subassembly includes the locking latch and the second seal subassembly includes the locking recess and the locking surface.
18. The surgical system according to claim 17 wherein the first seal subassembly includes a plurality of locking latches and the second seal subassembly includes a plurality corresponding locking recesses for receiving the locking latches.
19. A method for performing a surgical procedure, comprising the steps of:
providing an access assembly including an access housing and an access sleeve operatively connected to the access housing the access housing having a manual lock member;
mounting a seal assembly to the access housing, the seal assembly including a seal housing and a seal member mounted relative to the seal housing, the seal member including inner portions adapted to form a substantial seal about a surgical object introduced therethrough; and
securing the seal housing relative to the access housing by moving the manual lock member to cause corresponding structure of the access housing and the seal housing to cooperatively engage in secured relation therewith.
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
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US11/097,550 US20060020281A1 (en) | 2000-10-13 | 2005-04-01 | Valve assembly including diameter reduction structure for trocar |
AU2006201294A AU2006201294B2 (en) | 2005-04-01 | 2006-03-28 | Valve assembly including diameter reduction structure for trocar |
DE602006019513T DE602006019513D1 (en) | 2005-04-01 | 2006-03-29 | Sealing arrangement with two assemblies to be connected detachably |
EP06006538A EP1707135B1 (en) | 2005-04-01 | 2006-03-29 | Seal assembly including releasably connected first and second subassemblies |
EP10183545A EP2269523A1 (en) | 2005-04-01 | 2006-03-29 | Seal assembly including releasably connected first and second subassemblies |
CA002541307A CA2541307A1 (en) | 2005-04-01 | 2006-03-30 | Valve assembly including diameter reduction structure for trocar |
JP2006100823A JP2006280959A (en) | 2005-04-01 | 2006-03-31 | Valve assembly including diameter reducing structure for trocar |
US12/202,857 US7744569B2 (en) | 2000-10-13 | 2008-09-02 | Valve assembly including diameter reduction structure for trocar |
US12/824,528 US8282603B2 (en) | 2000-10-13 | 2010-06-28 | Valve assembly including diameter reduction structure for trocar |
JP2011159402A JP2011251138A (en) | 2005-04-01 | 2011-07-20 | Valve assembly including diameter reduction structure for trocar |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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US24050600P | 2000-10-13 | 2000-10-13 | |
PCT/US2001/031911 WO2002030305A2 (en) | 2000-10-13 | 2001-10-12 | Valve assembly including diameter reduction structure for trocar |
US10/380,942 US7025747B2 (en) | 2000-10-13 | 2001-10-12 | Valve assembly including diameter reduction structure for trocar |
US11/097,550 US20060020281A1 (en) | 2000-10-13 | 2005-04-01 | Valve assembly including diameter reduction structure for trocar |
Related Parent Applications (3)
Application Number | Title | Priority Date | Filing Date |
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US10380942 Continuation-In-Part | 2001-10-12 | ||
US10/380,942 Continuation-In-Part US7025747B2 (en) | 2000-10-13 | 2001-10-12 | Valve assembly including diameter reduction structure for trocar |
PCT/US2001/031911 Continuation-In-Part WO2002030305A2 (en) | 2000-10-13 | 2001-10-12 | Valve assembly including diameter reduction structure for trocar |
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US12/202,857 Continuation US7744569B2 (en) | 2000-10-13 | 2008-09-02 | Valve assembly including diameter reduction structure for trocar |
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US12/202,857 Expired - Fee Related US7744569B2 (en) | 2000-10-13 | 2008-09-02 | Valve assembly including diameter reduction structure for trocar |
US12/824,528 Expired - Fee Related US8282603B2 (en) | 2000-10-13 | 2010-06-28 | Valve assembly including diameter reduction structure for trocar |
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Application Number | Title | Priority Date | Filing Date |
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US12/202,857 Expired - Fee Related US7744569B2 (en) | 2000-10-13 | 2008-09-02 | Valve assembly including diameter reduction structure for trocar |
US12/824,528 Expired - Fee Related US8282603B2 (en) | 2000-10-13 | 2010-06-28 | Valve assembly including diameter reduction structure for trocar |
Country Status (6)
Country | Link |
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US (3) | US20060020281A1 (en) |
EP (2) | EP1707135B1 (en) |
JP (2) | JP2006280959A (en) |
AU (1) | AU2006201294B2 (en) |
CA (1) | CA2541307A1 (en) |
DE (1) | DE602006019513D1 (en) |
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EP1707135A1 (en) | 2006-10-04 |
JP2006280959A (en) | 2006-10-19 |
US7744569B2 (en) | 2010-06-29 |
CA2541307A1 (en) | 2006-10-01 |
AU2006201294B2 (en) | 2011-06-16 |
US20080319396A1 (en) | 2008-12-25 |
US20100331783A1 (en) | 2010-12-30 |
EP1707135B1 (en) | 2011-01-12 |
DE602006019513D1 (en) | 2011-02-24 |
EP2269523A1 (en) | 2011-01-05 |
US8282603B2 (en) | 2012-10-09 |
AU2006201294A1 (en) | 2006-10-19 |
JP2011251138A (en) | 2011-12-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
AS | Assignment |
Owner name: TYCO HEALTHCARE GROUP, LP, CONNECTICUT Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:SMITH, ROBERT C.;REEL/FRAME:017068/0600 Effective date: 20051001 |
|
STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |