|Publication number||US20060000869 A1|
|Application number||US 11/130,859|
|Publication date||5 Jan 2006|
|Filing date||17 May 2005|
|Priority date||17 May 2004|
|Also published as||CA2566794A1, EP1746940A2, US7585307, US20050283191, US20100224668, US20130087596, WO2005115254A2, WO2005115254A3|
|Publication number||11130859, 130859, US 2006/0000869 A1, US 2006/000869 A1, US 20060000869 A1, US 20060000869A1, US 2006000869 A1, US 2006000869A1, US-A1-20060000869, US-A1-2006000869, US2006/0000869A1, US2006/000869A1, US20060000869 A1, US20060000869A1, US2006000869 A1, US2006000869A1|
|Original Assignee||Datascope Investment Corp.|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (33), Referenced by (42), Classifications (18), Legal Events (1)|
|External Links: USPTO, USPTO Assignment, Espacenet|
The present application claims the benefit of U.S. Provisional Patent Application Ser. No. 60/571,738 filed May. 17, 2004, the disclosure of which is hereby incorporated by reference herein.
The present invention relates generally to a surgical stapling system, and more particularly to a system for joining two tubular structures using surgical staples. Still more particularly, the present invention relates to an apparatus and method for stapling together two tubular structures either through an open surgical procedure or laparoscopically.
The repair of aortic aneurysms and other aortic defects typically requires major abdominal surgery in which the defective segment of the aorta is removed and replaced with a prosthetic device, such as a synthetic graft. Such procedure ordinarily requires the graft to be sutured to the end of the sectioned aorta or to a felt cuff which has been sutured to the aorta. The suturing of the graft to the aorta or the cuff can be a difficult and time-consuming process, requiring the patient's aorta to be clamped shut for extended periods of time.
There therefore exists a need for an arrangement which will enable a tubular graft to be attached to the sectioned aorta in a quick and reliable manner.
The present invention addresses these needs.
The present invention provides a surgical stapler for joining a tubular prosthetic graft to a body lumen, the surgical stapler including a handle having a proximal end and a distal end; a loading unit removably connected to the distal end of the handle, the loading unit including a body adapted for insertion into the prosthetic graft; an anvil assembly having an open position and a closed position, the anvil assembly in the closed position being spaced around and relatively close to the body of the loading unit, and the anvil assembly in the open position being spaced relatively distant from the body of the loading unit; a plurality of staples arranged in the body of the loading unit for deployment along paths extending radially outward from the loading unit; a deployment mechanism operable to urge the plurality of staples outward from the loading unit along the radial paths; and an actuating mechanism at the proximal end of the handle and operable to actuate the deployment mechanism, whereupon the plurality of staples are simultaneously urged radially outward from the loading unit along the radial paths.
The loading unit may include a plurality of prongs arranged radially in the body, the prongs having a recessed position within the body for inserting the body into the prosthetic graft, and an extended position projecting radially outward from the body for holding the prosthetic graft in an assembled position on the loading unit.
The plurality of prongs may be connected to a first annular ring, and displacement of the first annular ring in an axial direction in the loading unit may move the plurality of prongs between the recessed position and the extended position.
The loading unit may include a distal end remote from the handle and at least one aperture in the distal end, the surgical stapler further including a loading tool insertable in the aperture to move the annular ring in the axial direction.
The loading unit may further include a plurality of fingers arranged radially in the body, the fingers having a recessed position within the body for inserting the body into the prosthetic graft, and an extended position projecting radially outward from the body for engaging an end edge of the prosthetic graft to hold the prosthetic graft in the assembled position on the loading unit.
The plurality of fingers may be connected to a second annular ring, and displacement of the second annular ring in the axial direction in the loading unit may move the plurality of fingers between the recessed position and the extended position. Preferably, insertion of the loading tool in the aperture moves both the first and second annular rings in the axial direction.
The plurality of staples may be arranged in a circumferential pattern in the body of the loading unit. In a preferred embodiment, the loading unit extends in an axial direction, and the plurality of staples are aligned in a plane orthogonal to the axial direction.
The surgical stapler may further include a control mechanism operable to move the anvil assembly between the open position and the closed position.
A more complete appreciation of the subject matter of the present invention and the various advantages thereof can be realized by reference to the following detailed description in which reference is made to the accompanying drawings in which:
In the detailed description which follows, the features of the present invention will be described in connection with the anastomosis of a prosthetic graft to the aorta, such as may be performed in the repair of an abdominal aortic aneurysm. It will be appreciated, however, that the various features of the present invention may be readily utilized to connect a tubular prosthetic graft to any body lumen. Each of the various components of the surgical stapling system of the present invention is described in separate headings below.
A generally cylindrical side port 20 is provided on one side of main body 12, generally between legs 14 and 16. Side port 20 provides a feature by which graft 10 may be inserted into a patient and held in place during a stapling procedure. In that regard, side port 20 preferably projects from graft 10 at an acute angle relative to legs 14 and 16 to facilitate the insertion of a loading unit 100 (see
Graft 10 is preferably formed from a biocompatible material having sufficient strength to withstand the surgical implantation procedure described more fully below, as well as the blood flow and other biomechanical forces which will be exerted on the graft. Such materials may include, for example, polyester materials, such as DACRONŽ, polytetrafluoroethylene, expanded polytetrafluoroethylene, polyester materials coated with polytetrafluoroethylene, polyurethane, expanded polyurethane and silicone.
Graft 10 may be provided in a range of sizes sufficient to accommodate the arterial morphology which the surgeon is likely to face in the vast majority of patients. In that regard, graft 10 may be provided with a cuff 18 having a diameter of approximately 16 m, 18 mm or 20 mm, although grafts 10 having larger or smaller diameters are also possible.
A second embodiment of a prosthetic graft 50 for use in the surgical stapling system of the present invention is shown in
It will be appreciated that the surgical stapling system of the present invention may make use of a graft having neither a side port 20 nor a flap 52. Rather, a graft having simply a cuff 18 at one end and a pair of legs 14 and 16 at the other end may be used.
A loading unit 100 for use in connection with the present invention is shown in
Referring to the exploded views of
At its distal end, cartridge 110 mates with a second cylindrical cartridge 120. Cartridge 120 has a central aperture 122 which aligns with aperture 114 of cartridge 110, and a plurality of radially extending slots 124, each of which aligns with a corresponding slot 116 in the distal end of cartridge 110 for receiving the elongated fingers 176 of actuator 170. A plurality of projections (not shown) on the proximal surface of cartridge 120 mate with corresponding recesses (not shown) formed in the end member 112 of cartridge 110 so as to maintain cartridge 120 in registry with cartridge 110.
A plurality of staple pushers 130 are arranged between cartridge 110 and cartridge 120 for radial sliding movement between an inner staple holding position and an outer staple ejecting position. The number of staple pushers 130 utilized will depend on the number of staples to be simultaneously deployed during a stapling procedure. The preferred embodiment of the invention described herein includes ten staple pushers 130 for deploying twenty staples. It will be appreciated, however, that a greater or lesser number of staple pushers may be utilized depending on the number of staples to be deployed and physical constraints dictated by the size and operation of loading unit 100.
Each staple pusher 130 has a generally U-shaped profile consisting of first and second legs 132 and 134 connected by an intermediate portion 136. Intermediate portion 136 has a first laterally projecting tab 138 which slidably engages in one of a plurality of recessed channels 140 formed in the end member 112 of cartridge 110. Recessed channels 140 coincide with radially projecting slots 116, but are larger in width and length. The opposite side of intermediate portion 136 has a second laterally projecting tab 142 which slidably engages in one of radial slots 124 formed in cartridge 120. Tab 142 projects from intermediate portion 136 adjacent the inner end 144 of staple pusher 130. Tab 138, on the other hand, projects from intermediate portion 136 at a spaced distance from end 144 of staple pusher 130. A recessed slanted cam surface 146 is formed in intermediate portion 136 between tabs 138 and 142, the purpose of which will be described below.
Prior to a stapling operation, with staple pushers 130 in their inner staple holding positions, loading unit 100 includes a plurality of surgical staples 150. Staples 150 are loaded in loading unit 100 so that the crossmember 152 of each staple rests against the free end of one of legs 132, 134 of staple pushers 130, with staple legs 154 and 156 projecting radially outward. More particularly, the crossmember 152 of each staple rests in an elongated recess 148 formed in the free ends of the legs 132 and 134 of each staple pusher 130. Further, the legs 156 and 154 of staples 150 reside within opposed radially extending guide channels 158 and 160, respectively, guide channels 158 being formed in end member 112 of cartridge 110, and guide channels 160 being formed in cartridge 120. Recesses 148 locate the staples and hold them in place with respect to the free ends of legs 132 and 134, while guide channels 158 and 160 guide the staples as they are deployed from loading unit 100. It will be appreciated from the foregoing that a loading unit 100 having ten staple pushers 130, and therefore twenty legs 132, 134, will be able to simultaneously deploy twenty staples 150.
Legs 132, 134 of staple pushers 130 each include a pair of lateral ribs 162 positioned in linear alignment with recess 148. Ribs 162 are aligned substantially colinearly with legs 154 and 156 of staples 150 so that, upon outward radial movement of staple pushers 130, the force exerted by the staple pusher is distributed along the entire length of crossmember 152, with a portion of the force being exerted in substantial linear alignment with the staple legs. As a result, any resistance to this outward movement as the free ends of staple legs 154 and 156 contact and pierce the aorta and graft 10 and strike the stapling anvils (to be described below) will not result in significant distortion to crossmember 152.
Staple pushers 130 are moved from their inner staple holding positions to their outer staple ejecting positions by actuator 170. Actuator 170 has a generally tubular main body 172 with an annular flange 174 at the proximal end thereof, and a plurality of elongated fingers 176 at the distal end thereof. Fingers 176 are sized and shaped to be slidably received in the slots 116 of cartridge 110 and the slots 124 of cartridge 120. Each of fingers 176 includes a tapered surface 178 which cooperates with the cam surface 146 of a corresponding staple pusher 130 to move the staple pusher radially outward during a stapling operation, as will be described below.
Actuator 170 is mounted on a tubular shaft 180 for sliding movement in the axial direction of loading unit 100. Shaft 180 has an enlarged annular flange 182 at its proximal end to prevent cap 104 from sliding axially beyond the proximal end of the shaft. A retaining clip 184 is assembled over a pair of transverse slots 186 formed in the main body 172 of actuator 170 and cooperates with an annular groove 188 formed in shaft 180 to temporarily prevent actuator 170 from sliding on shaft 180. The spring force of retaining clip 184 is only sufficient to prevent the unintended relative movement of actuator 170 on shaft 180 during shipping and handling of loading unit 100. During a stapling operation, however, the force exerted axially on actuator 170 is sufficient to overcome the spring force of retaining clip 184. That is, during a stapling operation, the axial force exerted on actuator 170 causes retaining clip 184 to spread open as it is pushed against the side of annular groove 188 until the retaining clip is pushed out of the groove, thereby enabling actuator 170 to slide axially along shaft 180. A pair of cutouts 185 are formed on the opposite sides of shaft 180 near its proximal end, the purpose of which will be discussed below.
Between cartridge 120 and cap 106, loading unit 100 includes an assembly for gripping the distal edge of graft 10 and holding it in place during shipment of the stapling system of the present invention and during a stapling procedure. The assembly includes an external graft retainer 190 having a plurality of fingers 192 which may be extended radially outward from loading unit 100 to grip the outer distal edge of graft 10, and an internal graft retainer 220 having a plurality of fingers 222 which may be extended radially outward from the loading unit to pierce the inner distal edge of graft 10. Retainers 190 and 220 are assembled over the shaft of an elongated screw 200 which extends through an aperture in cap 106, the central apertures in cartridges 110 and 120, and actuator 170, and which ultimately connects at its proximal end to the distal end of shaft 180 to hold all of the components of loading unit 100 in assembled relationship. Screw 200 may be joined to shaft 180 by any technique, including, for example, threaded engagement.
External graft retainer 190 includes a generally flat, circular hub 194 having a central aperture 196 for receiving the shaft of screw 200. Fingers 192 may be formed integrally with hub 194 and extend in a direction proximally and radially outward thereof. Each finger 192 terminates in a generally L-shaped tip 198 having a surface 198 a extending in a generally radial direction and a surface 198 b extending proximally therefrom in a generally axial direction. An angled cam surface 202 provided between tip 198 and hub 194 includes a protruding portion or bump 203 at the end of the cam surface farthest from tip 198. Retainer 190 is preferably formed from spring steel or a similar material and shaped so that fingers 192 will be biased toward their rest positions when displaced radially outward therefrom.
A cam ring 208 is mounted to hub 194 of retainer 190 by a plurality of screws or other known fastening technique, with a spring member 210 sandwiched therebetween. Cam ring 208 has an elongated central aperture 212 and a shaped surface 214 along its outer periphery. More particularly, the outer periphery of cam ring 208 includes a smaller diameter annular surface 208 a, a larger diameter annular surface 208 b, and a tapered surface 208 c therebetween, the purpose of which surfaces will be described below. Spring member 210 has a generally flat body portion 216 and a pair of tabs 218 bent in a proximal direction. Tabs 218 reside in an annular channel 201 formed in the shaft of screw 200, thereby limiting the amount by which retainer 190 may move in the axial direction.
Internal graft retainer 220 includes a generally flat circular hub 224 having an enlarged opening 226. opening 226 has enlarged regions which receive bosses 240 projecting from the interior of cap 106. Bosses 240 are undercut so that retainer 220 may be rotated relative to cap 106 to lock it in place on the interior of the cap.
Fingers 222 of retainer 220 may be formed integrally with hub 224 and extend in a direction proximally and radially outward thereof. Each finger 222 terminates in a needle-like tip or prong 228 which projects radially outward. A radially inward projecting cam 230 formed on each finger 222 intermediate tip 228 and hub 224 has an angled distal cam surface 230 a, a cam surface 230 b which extends generally in the axial direction, and an angled proximal cam surface 230 c. Cam 230 is adapted to cooperate with the shaped peripheral surface 214 of cam ring 208 as will be described further below. Retainer 220 is preferably formed from the same spring steel or similar material as retainer 190 and shaped so that fingers 222 will be biased toward their rest positions when displaced radially outward therefrom.
In the assembled condition of loading unit 100, retainers 190 and 220 are positioned relative to one another so that each finger 192 of retainer 190 lies adjacent a finger 222 of retainer 220. Each pair of fingers 192, 222 resides in one of a plurality of radial recesses 242 formed in the distal surface of cartridge 120 and continuing in the proximal surface of cap 106. Each recess 242 includes a first surface 242 a extending generally in an axial direction, and a cam surface 242 b extending at an angle to surface 242 a. The surfaces 242 a and 242 b of each recess 242 are intended to interact with the cam surface 202 and bump 203 of the finger 192 residing in that recess, as will be explained further below.
A guidewire 250 is connected at one end to loading unit 100 and projects outward from the proximal end thereof. Guidewire 250 has an enlarged end 252 formed in a conventional fashion. End 252 is receivable in a slot 254 having an enlarged end 256 formed in the shaft of screw 200. The guidewire then extends through an axial bore (not shown) in the shaft of screw 200, through the hollow center of shaft 180 and out the proximal end of loading unit 100. The engagement of the enlarged end 252 of guidewire 250 in the enlarged end 256 of slot 254 locks the guidewire in place and prevents it from being pulled proximally out from loading unit 100.
A procedure will now be described for mounting a graft 10 onto loading unit 100, which procedure is typically performed in a factory prior to shipment of the stapling system of the present invention.
In this initial condition, loading unit 100 may be inserted into side port 20 of graft 10 until the distal end of cartridge 110 protrudes from cuff 18. With graft 10 being held in this position, an actuating tool T may be used to advance retainer 190 to the loading position shown in
The proximal movement of retainer 190 also causes cam ring 208 to move proximally, whereupon the proximal edge of the cam ring will ride along the cam surfaces of the cams 230 on fingers 222 until cam surfaces 230 c slide down tapered surface 208 c on the cam ring and cam surfaces 230 b come to rest on smaller diameter annular surface 208 a. As in the initial starting position, the tips 228 of fingers 222 will be positioned below the outer surface of loading unit 100.
With fingers 192 and 222 in these positions, graft 10 can be positioned so that the free edge of cuff 18 rests against surface 198 a and below surface 198 b at the tip of each finger 192. At this point, actuating tool T may be moved in the direction of arrows B shown in
In either event, as retainer 190 moves distally, cam ring 208 moves distally with it. This movement causes the cam surfaces 230 c on fingers 222 to ride up the tapered surface 208 c on cam ring 208, with cam surfaces 230 b ultimately coming to rest on larger diameter annular surface 208 b. This action causes fingers 222 to expand radially outward of loading unit 100 so that the tips 228 thereof pierce graft 10 from the inside. The interaction of the tips 198 of fingers 192 and the tips 228 of fingers 222 with graft 10 hold the graft securely on loading unit 100. That is, with tabs 218 of spring member 210 abutting the distal wall of annular channel 201, retainer 190 is prevented from moving further in the distal direction. Furthermore, the interaction of the bumps 203 on fingers 192 with cam surfaces 242 b prevents retainer 190 from moving proximally in the axial direction since any such movement would have to overcome the biasing force of fingers 192. With retainer 190 unable to move axially in either direction, the tips 198 of fingers 192 and the tips 228 of fingers 222 remain in fixed positions and hold graft 10 securely in place. An elevational view of the loading unit 100 having a graft 10 loaded thereon is shown in
In a variant of loading unit 100 described above, rather than relying upon the relative biasing forces exerted by fingers 192 and 222, or upon an optional spring assembled between cam ring 208 and cartridge 120, the pins P of actuating tool T may be provided with a feature which engages a corresponding feature in the hub 194 of retainer 190 so that actuating tool T may be used to manually pull retainer 190 distally to an appropriate position.
It will be appreciated that loading unit 100 may be provided in a series of different diameters which correspond to the diameters in which graft 10 is provided. Thus, graft 10 and loading unit 100 are typically provided as a unit, with graft 10 mounted on a loading unit in condition for ready use by the surgeon.
Also, loading unit 100 may be formed as a reusable device, including components formed from spring steel and other relatively expensive materials. Alternatively, loading unit 100 may be formed from less costly materials, such as plastic, so as to be disposable after a single use.
An attachment mechanism 314 is connected to the distal end of shaft 302. Attachment mechanism 314 has a cylindrical end portion 316 having a counterbore sized for receiving the distal end of shaft 302. A flat may be formed in the counterbore so as to mate with a corresponding flat formed on the distal end of shaft 302, thereby defining the proper rotational relationship between attachment mechanism 314 and shaft 302. Attachment mechanism 314 may be held in assembled relationship on shaft 302 by a set screw (not shown) or any other known fastening technique.
Projecting distally from end portion 316 of attachment mechanism 314 is an elongated finger 320. Finger 320 has a pair of flat side surfaces 322, a curved upper surface 326 and a flat lower surface. The shapes of these surfaces coincide with the internal shape of shaft 180 of loading unit 100 so that the loading unit is unable to rotate once assembled to wand 300. A bore (not shown) extending through attachment mechanism 314 aligns with bore 308 in shaft 302 when these components are assembled together.
At its proximal end, wand 300 includes an operating handle 330 having first and second handle portions 332 and 334 which may be assembled together using any conventional technique. Handle 330 may be assembled to the proximal end of shaft 302 by capturing a reduced diameter portion 336 of shaft 302 between the handle portions when they are assembled together. A pair of projections 338 and 340 formed in each of handle portions 332 and 334 engage a pair of grooves 342 and 344, respectively, formed transversely in shaft 302 to locate shaft 302 in the proper rotational orientation relative to handle 330 and to prevent the shaft from sliding out of the handle when in the assembled position. Coiled guidewire tubing 346 is held in the proximal end of handle 330 by the assembly of handle portions 332 and 334. Guidewire tubing 346 receives the excess length of guidewire 250 which protrudes out from the proximal end of wand 300 and holds it in a manageable position. When wand 300 is removed from loading unit 100, as explained below, coiled tubing 346 may first be removed from handle 330 by pulling to expose guidewire 250. Alternatively, guidewire tubing 346 may remain connected to handle 330, and guidewire 250 may simply be pulled out from the tubing as wand 300 is removed from loading unit 100.
Handle 330 includes a locking mechanism 350 operable between a locked position for engaging guidewire 250 so as to prevent sliding movement between wand 300 and the guidewire, and an unlocked position for releasing the wand for movement relative to the guidewire. In the embodiment shown in
More particularly, in the locked condition of locking mechanism 350, button 354 is in the depressed position shown in
Depressing button 356 to move trigger lock 352 to the unlocked position shown in
A second embodiment of a placement wand 380 for use with the present invention is shown in
In the locked condition of locking mechanism 382, the trigger lock 384 is slid to the distal position shown in
Sliding trigger lock 384 in the proximal direction to the unlocked position shown in
Surgical loop 400 has a generally straight hollow shaft 402 with a handle 404 provided at a proximal end thereof. A button 406 is mounted in handle 404 for sliding movement in an axial direction along an elongated slot 408. Within handle 404, button 406 is connected to the proximal end of an elongated rod 410 which is arranged for sliding movement within shaft 402.
At its distal end, shaft 402 is enclosed by an end plug 412 having a through slot 414. Through slot 414 is sized to slidably receive an elongated flexible band 416. At one end, band 416 is fixedly connected to the distal end of rod 410, such as by a screw 417 or any other conventional connecting technique. At its other end, band 416 has a rounded tip 418 and opposed notches 420 defining a narrowed neck spaced from tip 418, the purpose of which will be described below. Band 416 preferably is wider than it is thick so as to define a rectangular cross-section which will hold an annular shape better than the round cross-section of a conventional suture. Band 416 may be formed from any material having sufficient flexibility to conform smoothly around loading unit 100, graft 10 and the aorta, and sufficient tensile strength to securely hold graft 10 and the aorta in overlapping relationship during a stapling operation. In that regard, particularly preferred materials for forming band 416 are nitinol or other shape memory materials, polypropylene, polyethylene, Mylar™ polyester, nylon and other suitable materials. Nitinol or other shape memory materials are particularly preferred since they permit band 416 to be preformed with a curvature that will facilitate the maneuvering of band 416 around the graft and artery.
A retaining block 422 is assembled in the distal end of shaft 402 for sliding movement in the axial direction between end plug 412 and one or more tangs 424 bent inwardly from shaft 402. A spring 426 disposed between retaining block 422 and end plug 412 biases the retaining block in the proximal direction against tangs 424.
Retaining block 422 has an axial bore 428 which is sized and shaped to receive the rounded tip 418 of band 416. Below bore 428, retaining block 422 has an axial slot 430 aligned with the through slot 414 in end plug 412 and sized and shaped to receive band 416 for sliding movement relative to the retaining block. The upper wall 432 of retaining block 422 has an axial slot 434 which extends the length of the retaining block and communicates with axial bore 428. A keyhole 436 is formed in the upper wall 432 of retaining block 422 in a direction transverse to slot 434. Keyhole 436 is sized to receive tip 418 of band 416 and to permit its insertion into axial bore 428.
To operate surgical loop 400, button 406 is initially pushed in the distal direction to deploy band 416 through the slot 414 in end plug 412. When formed from a shape memory material, band 416 will form a curved shape so that tip 418 will approach the distal end of shaft 402. When not formed from a shape memory material, band 416 may be manually manipulated to place tip 418 near the distal end of shaft 402.
Surgical loop 400 may then be operated to capture the tip 418 of band 416. More particularly, button 406 may be pushed further in the distal direction so that the distal end of rod 410 contacts retaining block 422. Further movement of button 406 in the distal direction will cause rod 410 to push retaining block 422 in the distal direction against the biasing force of spring 426 until the keyhole 436 in retaining block 422 is aligned with an aperture 438 in shaft 402. At this point, tip 418 of band 416 may be inserted through aperture 438 and keyhole 436 until the tip resides within the axial bore 428 in retaining block 422 and notches 420 are aligned with the slot 434 in the upper wall 432 of the retaining block. As button 406 is released, the biasing force of spring 426 will push retaining block 422 proximally, whereupon notches 420 will reside in slot 434, keyhole 436 will no longer be aligned with aperture 438 and tip 418 will be captured within the bore 428 in the retaining block.
To tighten band 416 around loading unit 100, graft 10 and the aorta, button 406 is moved in the proximal direction so as to draw band 416 into shaft 402. As button 406 is retracted, a plurality of teeth (not shown) provided on button 406 may engage with a similar plurality of teeth (not shown) provided on handle 404. The engagement of the teeth on these respective components may act as a ratchet mechanism enabling button 406 to be retracted, but blocking it from movement relative to handle 404 in the distal direction. Therefore, as band 416 is progressively tightened, it will be locked in place and prevented from loosening at each step in the tightening process. The teeth on the respective components may be biased into engagement with one another by a spring (not shown) interposed between button 406 and handle 404. Thus, by depressing button 406 to overcome the biasing force of the spring, the teeth may be separated from one another so that button 406 may be moved distally to release band 416.
Rather than employing a band 416 having a rectangular cross-section, surgical loop 400 may employ a conventional wire having a round cross-section. In such event, the wire would include an enlarged feature at its distal end which may be captured and held within bore 428 in retaining block 422.
One embodiment of a stapling instrument 500 which attaches to loading unit 100 and is operable to actuate a stapling procedure is illustrated in
Referring specifically to
The brackets 524 on the ends of anvils 518 a, 518 b and 518 c each define an arc such that, in the closed position of anvil assembly 510, these brackets collectively define a complete circle. Each bracket 524 includes a male locating member 530 at one end thereof and a female locating member 532 at the opposite end thereof, the male and female locating members on adjacent brackets 524 engaging with one another in the closed position of anvil assembly 510 so as to properly locate and align staple returns 528 relative to one another.
In a preferred embodiment hereof shown in
Anvils 518 a, 518 b and 518 c are pivotably mounted to anvil hub 514 by a series of yokes 534 formed at spaced distances on the outer surface of side wall 516. Each yoke 534 includes a pair of supports 536 which project beyond the distal end 538 of anvil hub 514, and which are spaced apart so as to receive one of anvil arms 520 therebetween. A barrel nut 540 may be inserted through a pair of axially aligned apertures 542 formed in supports 536 and through an aperture 544 provided at the dog leg in an anvil arm 520 and mate with a screw 541 for holding the anvil in assembled relationship to anvil hub 514. Alternatively, anvils 518 may be held to yokes 534 through any other technique allowing pivoting of the anvil arms, such as through a pivot pin or the threaded engagement of one end of a shoulder bolt with threads formed in one of apertures 542. Access openings 546 are formed in side wall 516 in the spaces between each pair of supports 536 in a yoke 534, the access openings continuing radially inward by a predetermined amount in the distal end 538 of anvil hub 514. Access openings 546 enable the proximal ends of anvil arms 520 to project into the interior of anvil hub 514 and provide clearance for the movement of anvils 518 between open and closed positions. The distal end 538 of anvil hub 514 includes a central aperture 545 having curved top and bottom surfaces and flat side surfaces, and a series of apertures 548 arranged substantially symmetrically around central aperture 545 for slidably receiving the fingers of a pusher 600, the purpose of which will be described below.
A cam element 550 is slidably assembled in the open proximal end of anvil hub 514. Cam element 550 has a generally cylindrical structure with a series of ribs 554 projecting radially outward therefrom. Ribs 554 are oriented in the axial direction of anvil assembly 510 and engage in similarly oriented channels (not shown) formed in the interior of anvil hub 514. Each channel is positioned so as to be radially inward of a corresponding yoke 534.
Ribs 554 are formed with a central slot 558 having a width sufficient to receive the proximal end of an anvil arm 520, and an undercut 560 on each side of the slot for receiving the guide pins 522 on anvils 518. The bottom surface of each slot 558, including undercut portions 560, defines a tapered cam surface 562 so that axial movement of cam element 550 relative to anvil hub 514 causes anvils 518 to move between the open and closed positions. An arm 564 projects axially from the proximal end of cam element 550. Arm 564 has a transverse aperture 566 at its free end for connection to a drive mechanism for effecting axial movement of cam element 550, as will be explained below.
Cam element 550 includes a central bore 568 having flat top and bottom surfaces and curved side surfaces, and a generally cylindrical counterbore 570 extending inwardly from the distal end of the cam element to an end wall 572. A series of through openings 574, similar in size and shape to apertures 548 in anvil hub 514, are arranged substantially symmetrically around central opening 568 for slidably receiving the fingers of pusher 600.
An anvil hub shaft 576 is mounted in anvil assembly 510 between anvil hub 514 and cam element 550. Shaft 576 has a large intermediate portion 578 having a substantially cylindrical cross-section, and a proximal end portion 580 which is smaller in cross-section so as to define a step 582 therebetween. Similarly, shaft 576 has a distal end portion 584 which is smaller in cross-section than intermediate portion 578 so as to define a step 586 therebetween. The intermediate portion 578 of shaft 576 has similar recesses 588 formed in its upper and lower surfaces, each of which is sized and shaped to receive a catch member 590. Catch members 590 have a protruding transverse rib 591 so that the catch members rest in recesses 588 in a see-saw fashion. A spring catch 592 in the form of a split ring may be assembled in an annular groove 594 formed by the circumferential alignment of groove portions in the intermediate portion 578 of shaft 576 and in each of catch members 590. The assembly of spring catch 592 around the catch members 590 and the intermediate portion 578 of shaft 576 holds the catch members in assembled relationship to shaft 576 so that the distal ends of the catch members are biased outwardly, while permitting the distal ends of the catch members to pivot inwardly upon the application of a radially inward compressive force thereto. At their distal ends, catch members 590 each have a radially projecting prong 596 having a sharply tapered distal surface and a slightly tapered proximal catch surface. Prongs 596 secure loading unit 100 to instrument 500, as will be explained below.
The distal end portion 584 of shaft 576 has a shape similar to that of the elongated finger 320 at the end of wand 300. That is, the distal end portion 584 of shaft 576 has flat side and lower surfaces and a curved upper surface for mating engagement within shaft 180 of loading unit 100. An axial bore 599 is provided along the length of shaft 576 for receiving guidewire 250, as will be explained below.
Shaft 576 is assembled in anvil hub 514 so that the distal end portion 584 of shaft 576 extends through the central aperture 545 in the anvil hub, with step 586 abutting the inside wall of the distal end 538 of the anvil hub adjacent aperture 545. The shape of the aperture 545 in anvil hub 514 assures that the anvil hub is assembled in the proper orientation on shaft 576 and is unable to rotate once assembled thereon. In this assembled position, the distal end portion 584 of shaft 576 extends outwardly from anvil hub 514, as do the radially projecting prongs 596 on catch members 590.
Cam element 550 is assembled in anvil hub 514 so as to capture the intermediate portion 578 of shaft 576 therebetween. That is, cam element 550 is assembled over the proximal end portion 580 of shaft 576 until the end wall 572. of counterbore 570 is engaged with step 582 on shaft 576. The corresponding shapes of the proximal end portion 580 of shaft 576 and the central bore 568 in cam element 550 assures that these elements are assembled in the proper orientation and that the cam element is unable to rotate once assembled on the shaft.
A pusher 600 having a disk-shaped base member 602 and a plurality of axially extending fingers 604 is assembled in anvil assembly 510 so that fingers 604 extend through openings 574 in cam element 550 and apertures 548 in anvil hub 514. Fingers 604 are of a sufficient length that when pusher 600 is displaced fully in the distal direction, the free ends of fingers 604 protrude outwardly from the distal end 538 of anvil hub 514 and into a loading unit 100 mounted on instrument 500. As will be explained below, pusher 600 acts on actuator 170 to deploy staples 150 during a stapling operation. A link 606 having a transverse aperture 608 is connected to the proximal end of base member 602 for joining pusher 600 to a drive mechanism for effecting axial movement of the pusher.
Anvils 518 may be moved between the open and closed positions by an adjustment knob 610 provided at the handle end of instrument 500. Adjustment knob 610 actuates a drive mechanism which transfers rotational movement of knob 610 into axial movement of cam element 550, thereby displacing anvils 518. Referring to
Link coupler 614 may be joined to arm 564 on cam element 550 by a plurality of links 620. A pair of track inserts 622 assembled in the opposite sides of curved distal end portion 506 of shaft 502 may define first and second pairs of laterally spaced guide tracks 624 and 626. Links 620 may ride in guide tracks 626 so that any axial movement of tube 612 is transferred along the curved portion of shaft 502 to cam element 550. Links 620 may take any form capable of transmitting the compressive force exerted by tube 612 and link coupler 614 to cam element 550 as anvil assembly 510 is placed in a closed condition, and capable of transmitting the tensile force from tube 612 and link coupler 614 to cam element 550 as tube 612 is retracted to place anvil assembly 510 in an open condition. Thus, links 620 may consist of individual links joined together in a conventional fashion, or may be in the form of a solid band having periodic thinned sections defining a plurality of living hinges. Alternatively, links 620 may not be links at all, but may be a solid band having the requisite compressive and tensile strength, while at the same time having sufficient flexibility to bend smoothly and uniformly along the curved portion of shaft 502.
At its proximal end, tube 612 may be connected to a coupling element 628. In a preferred embodiment, the proximal end of tube 612 may be inserted into a bore formed in the distal end of coupling element 628, and these elements may be held together in the same manner as tube 612 and link coupler 614, that is, by sliding a retaining ring (not shown) into a slot 630 formed transversely in coupling element 628 and engaging it in an annular groove formed adjacent to the proximal end of tube 612. Alternatively, the distal end of tube 612 may be joined to link coupler 614 and the proximal end of tube 612 may be joined to coupling element 628 by any other known connection techniques. Coupling element 628 may have a pair of elongated bosses (not shown) extending in the axial direction on either side of the coupling element. Each of the bosses may be slidably held in an elongated slot provided in each of handle portions 511 and 513. The elongated slots have a predetermined length so as to define the extent of axial travel of coupling element 628.
At its proximal end, coupling element 628 may be threadedly engaged with a shaft 642. Shaft 642 has a stepped structure so as to define an intermediate portion 644 which is smaller in diameter than a threaded distal portion 646 and larger in diameter than a proximal portion 648. A bushing 650 may be assembled over intermediate portion 644 and may be held in place by the step between the intermediate portion 644 and distal portion 646 of shaft 642 and a retaining ring 652 assembled in an annular groove formed in the intermediate portion 644 proximally of the bushing. The outer circumference of bushing 650 may be formed with an annular groove 654 which enables the bushing to be captured in a circular opening formed in the proximal end of handle 512 when handle portions 511 and 513 are assembled together.
Adjustment knob 610 has an internal elongated annular boss 656 for receiving the proximal portion 648 of shaft 642. A pair of diametrically opposed teeth 658 formed on the free end of boss 656 may engage recesses 660 formed in the intermediate portion 644 of shaft 642 so that any rotational movement of knob 610 results in a corresponding rotation of shaft 642. A barrel nut 662 engages a threaded portion 664 formed on the proximal portion 648 of shaft 642 so as to hold knob 610 in assembled relationship to the shaft. Barrel nut 662 resides in a counterbore 666 formed in the proximal end of knob 610 so that it does protrude outwardly from the knob.
Optionally, a conventional clutch mechanism (not shown) may be provided between knob 610 and shaft 642 to prevent the overloading of anvil assembly 510. Thus, once a threshold to the further closure of anvils 518 a, 518 b and 518 c has been met (either because the anvils are fully closed or because there is interfering tissue), the clutch mechanism will enable knob 610 to rotate without further movement of the anvils, thereby preventing damage to instrument 500 or damage to tissue from the closing anvils.
Handle 512 of instrument 500 is further provided with a trigger mechanism 670 for actuating a stapling operation. Referring to
An elongated tube 702 slidably disposed within outer shaft 502 of instrument 500 and over tube 612 may be connected at its proximal end to coupling element 694. More particularly, the proximal end of tube 702 may be inserted in a bore formed in the distal end of coupling element 694. This assembly may be maintained in the same manner as the assembly of tube 612 to link coupler 614, that is, by sliding a retaining ring (not shown) into a slot 703 formed transversely in coupling element 694 and engaging it in an annular groove formed adjacent to the proximal end of tube 702. At its distal end, tube 702 may be connected to a coupling link 704. In a preferred arrangement, the distal end of tube 702 may be inserted in a bore formed in the proximal end of coupling link 704 and may be held in assembled relationship therein in the same fashion as the other tube/coupler connections described above, namely, by sliding a retaining ring (not shown) into a slot 706 formed transversely in coupling link 704 and engaging it in an annular groove formed adjacent to the distal end of tube 702. Alternatively, any other known connection techniques may be used both to join the distal end of tube 702 to coupling link 704, and to join the proximal end of tube 702 to coupling element 694. Coupling link 704 preferably is assembled over tube 612 and proximally of link coupler 614 so as to not interfere with the axial movement thereof, and may be joined to link 606 on pusher 600 by a plurality of links 708. Links 708 may ride in laterally spaced guide tracks 624 formed in track inserts 622 so that any axial movement of tube 702 is transferred along the curved portion of shaft 502 to pusher 600. Links 708 may have any of the structures described above in connection with links 620. Moreover, links 708 may have the same structure as links 620 or a structure different therefrom.
As will be appreciated from the foregoing description, trigger mechanism 670 may be actuated by pressing trigger 672 toward handle 512. This movement of trigger 672 will cause engagement surface 700 to push against the apex 698 of linkage assembly 680, thereby causing the angle between links 682 and 684 to be increased against the biasing force of spring 696. Since the end 688. of linkage assembly 680 is fixed relative to handle 512, the increased angle between links 682 and 684 will cause the other end 692 of linkage assembly 680 to move axially in the distal direction. This axial movement will be transferred through coupling element 694, tube 702, coupling link 704 and links 708 to pusher 600, resulting in the movement of the fingers 604 of the pusher into loading unit 100 and the resultant deployment of staples 150. Following the deployment of staples 150, the biasing force of spring 696 will cause trigger 672 to return to its rest position as the compressive force is released therefrom.
Instrument 500 may further include a guidewire tube 709 which is positioned within tube 612. At its .distal end, guidewire tube 709 protrudes out from tube 612 and has a curved portion whose distal end is inserted in a counterbore formed in the proximal end of anvil hub shaft 576. At its proximal end, guidewire tube 709 extends out from tube 612, through coupling element 628 and into shaft 642. Guidewire tube 709 provides an uninterrupted channel for guidewire 250 from loading unit 100 through instrument 500.
To prevent the premature accidental deployment of staples 150, trigger mechanism 670 may be provided with a safety 710. Safety 710 may be in the form of an elongated pin (not shown) having a radially projecting tab 714 formed with an aperture 716. A shaft (not shown) may be inserted through aperture 716 to mount safety 710 for sliding movement in a transverse direction between handle portions 511 and. 513. A first spring (not shown) mounted on the shaft between tab 714 and handle portion 511, and a second spring (not shown) mounted on the shaft between tab 714 and handle portion 513 bias safety 710 to a rest position which is in a substantially central location between the handle portions. In this rest position, one end of the elongated pin projects outwardly through an aperture in handle portion 511 to define a first button, and the other end of the elongated pin projects outwardly through an aperture in handle portion 513 to define a second button. With the ends of the elongated pin and the shaft constrained from movement by handle portions 511 and 513, safety 710 is prevented from moving pivotably relative to handle 512, but is free to move transversely with respect to the handle. Safety 710 further includes a pair of tangs 732 which, in the rest position of the safety, align with and engage notches 734 formed in the side walls 676, respectively, of trigger 672. Such engagement prevents trigger 672 from being depressed to actuate a stapling operation. Pressing either the first or the second button toward handle 512 moves tangs 732 out of alignment with side walls 676 of trigger 672, thereby clearing the path for the trigger to be depressed relative to handle 512 so that a stapling operation can be performed.
A second embodiment of a handle and trigger mechanism for use with a stapling instrument 800 in accordance with the present invention is shown in
Instrument 800 includes the same tube 702, coupling link 704 and links 708 as instrument 500. However, the structure at the proximal end of tube 702 differs from that in instrument 500. More particularly, the proximal end of tube 702 may be connected to a coupling element 818 in any conventional manner, including that by which tube 612 is connected to coupling element 628 at its proximal end. Coupling element 818 may be assembled on tube 612 for sliding movement in the axial direction of the tube. A biasing spring 820 may be assembled over tube 702 between the distal end of coupling element 818 and an annular surface 822 formed transversely in handle 808. Coupling element 818 may have a pair of elongated bosses (not shown) extending in the axial direction on either side of the coupling element. Each of these bosses may be slidably held in an elongated slot (not shown) provided in each of handle portions 812. The elongated slots have a predetermined length so as to define the extent of axial travel of coupling element 818.
Drive portion 810 of trigger 804 may be formed with a pair of spaced walls 828 at the free end thereof. Each of walls 828 may include a curved cam surface 830 projecting in a distal direction therefrom. In the assembled position of trigger mechanism 802, walls 828 reside on either side of tube 612 with cam surfaces 830 contacting the proximal end of coupling element 818. In the rest position of trigger mechanism 802, shown in
Instrument 800 may further include a safety 840 to prevent the premature accidental deployment of staples 150. Safety 840 may be pivotably connected between handle portions 812 by a pivot pin 842 so that safety 840 is positioned between handle 808 and the grasping portion 806 of trigger 804. At its free end, safety 840 has a recess 844 sized to receive the grasping portion 806 of trigger 804. Recess 844 may include a resilient member 846 adapted to engage within a shallow recess 848 in grasping portion 806 in the locked condition of trigger mechanism 802. In a preferred embodiment, resilient member 846 may be in the form of an S-shaped member integrally molded with safety 840. Resilient member 846 causes safety 840 to fit tightly between handle 808 and grasping portion 806 in the locked condition. Such engagement prevents trigger 804 from being depressed to actuate a stapling operation. Pivoting safety 840 away from grasping portion 806, however, releases trigger 804 for movement toward handle 808 to actuate a stapling operation.
Sizer 900 includes a shaft 902 having a substantially straight elongated portion 904 and a distal end portion 906 which is oriented at an angle relative to elongated portion 904. End portion 906 may form an angle of between about 90° and about 180° with elongated portion 904. In preferred embodiments, end portion 906 forms an angle of between about 105° and about 125° with elongated portion 904, with an angle of about 115° being most preferred.
A handle 908 is provided at the proximal end of shaft 902, and a measuring bulb 910 is provided at the distal end of the shaft. Measuring bulb 910 has a cylindrical central portion 912 with a generally frusto-conical portion 914 formed on the distal end thereof and another generally frusto-conical portion 916 formed on the proximal end thereof adjacent shaft 902. The frusto-conical shape of portions 914 and 916 facilitate the insertion and removal of sizer 900 through a surgical opening, as well as the insertion of sizer 900 into a transected aorta.
As shown in
The length L dimension of bulb 910 is used to determine whether there is an adequate amount of transected aorta available between the surgical clamp on the aorta and the point of transection to perform a stapling procedure. Thus, if the bulb 910 of a sizer 900 can be inserted into the transected aorta so that the entirety of central portion 912 lies within the aorta, the length of aorta available will be sufficient to perform a stapling procedure. However, if a length of central portion 912 remains exposed when bulb 910 has been inserted fully within the transected aorta (i.e., until the surgical clamp prevents further insertion of the bulb), there will not be a sufficient length of aorta available to perform the stapling procedure. In such event, the surgical clamp may be moved farther away from the point of transection to make more of the aorta available. If that is not possible, a conventional graft may be attached to the aorta using a conventional suturing technique. Since the length of aorta available for a stapling procedure is independent of the diameter of the aorta, the length L is the same for each of bulbs 910, regardless of their diameters.
Bulb 910 is provided with a circumferential recess 920 in central portion 912. Recess 920 is located in the length direction of the bulb so as to indicate the position at which the circumferential line of staples will be deployed. Hence, a surgeon may position bulb 910 of sizer 900 adjacent the aorta prior to transecting same to ensure that the staples will be deployed in healthy aortic tissue relative to the point of transection.
The use of the surgical stapling system of the present invention to attach a graft to a transected aorta will be now be described with reference to
As a first step of the procedure, the surgeon may position a sizer 900 adjacent an aorta A to be repaired so as to determine, based on the anticipated point of transection, whether there will be healthy aortic tissue at the projected circumferential stapling line indicated by the circumferential recess 920 in the sizer. The surgeon may then clamp the aorta and form a transection as shown in
Once the approximate size of the aorta has been determined, and assuming the availability of a sufficient length of transected aorta, the surgeon uses wand 300 to insert a loading unit 100 and its associated graft 10 of the proper diameter into the transected aorta. Referring to
Once band 416 has been placed around the aorta and tightened, wand 300 may be disconnected from loading unit 100. This may be accomplished by first pulling guidewire tubing 346 from the proximal end of handle 330 and off of guidewire 250, and then depressing button 356 on handle 330 to place locking mechanism 350 in the unlocked condition. As a result, wand 300 may be pulled proximally along guidewire 250, whereupon finger 320 will be drawn out from shaft 180 of the loading unit 100. Wand 300 may then be removed entirely from guidewire 250. Alternatively, wand 300 may be removed from guidewire 250 with guidewire tubing 346 attached thereto.
As the next step, the surgeon may assemble instrument 500 to loading unit 100 as shown in
Anvil assembly 510 may then be placed in the closed condition shown in
With anvil assembly 510 fully closed, trigger mechanism 670 may be actuated to deploy staples 150. As a first step, one of buttons 726 and 730 is depressed to release safety 710 from trigger 672. Trigger 672 may then be squeezed toward handle 512, whereupon engagement surface 700 within trigger 672 pushes against the apex 698 of linkage assembly 680. This movement causes the end 692 of linkage assembly 680 to move axially in the distal direction, thereby moving coupling element 694, tube 702, coupling link 704 and links 708 distally. The distal movement of links 708 drives the fingers 604 of pusher 600 out through apertures 548 of anvil hub 514, through apertures 105 in the cap 104 of loading unit 100, and against the annular flange 174 at the proximal end of actuator 170.
The continued distal movement of pusher 600 drives actuator 170 distally, overcoming the spring force exerted by retaining clip 184 to hold actuator 170 in a fixed axial position relative to shaft 180. The distal movement of actuator 170 causes the tapered surface 178 on each of the fingers 176 of the actuator to engage the cam surface 146 of a corresponding staple pusher 130. As a result of the interaction of tapered surfaces 178 with staple pushers 130, the staple pushers are driven radially outward, pushing staples 150 ahead of them. Staples 150 move radially outward until the free ends of the legs 154 and 156 of the staples contact the staple returns 528 on anvils 518. Staple returns 528 cause staple legs 154 and 156 to turn inwardly and back toward the crossmember 152 of the staple so as to form a “CB” configuration, shown in
As the fingers 176 of actuator 170 progress distally, the tips of the fingers will engage the proximal surface of cam ring 208, driving the cam ring and retainer 190 connected thereto toward cap 106, as shown in
Following the deployment of staples 150, trigger 672 may be released, whereupon the biasing force of spring 698 will cause the trigger to return to its rest position. At the same time, the apex 698 of linkage assembly 680 will move away from handle 512, with the end 692 of the linkage assembly moving in the proximal direction. This proximal movement will cause coupling element 694, tube 702, coupling link 704 and links 708 to also move proximally, resulting in the withdrawal of the fingers 604 of pusher 600 from loading unit 100. Anvil assembly 510 may then be placed in the open condition by rotating knob 610 in the opposite direction, and instrument 500, with loading unit 100 connected thereto, may be removed from graft 10, leaving the graft attached to the aorta by a circumferential line of staples 999, as can be seen in
The various components of the present invention may be used in a conventional open body surgical procedure. The instruments may also be used to perform a stapling operation laparascopically by providing the instruments with appropriate seals to prevent the escape of air used to expand the body cavity during a laparoscopic procedure.
In addition to the several embodiments described above, the various components of the stapling system of the present invention may be varied in many ways. For example, it will be appreciated that, where appropriate, any of the features described in connection with a particular embodiment hereof may be incorporated in any other embodiment described herein.
Although the invention herein has been described with reference to particular embodiments, it is to be understood that these embodiments are merely illustrative of the principles and applications of the present invention. It is therefore to be understood that numerous modifications may be made to the illustrative embodiments and that other arrangements may be devised without departing from the spirit and scope of the present invention as defined by the appended claims.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US3561429 *||23 May 1968||9 Feb 1971||Eversharp Inc||Instrument for obtaining a biopsy specimen|
|US3735762 *||29 Dec 1971||29 May 1973||Us Corp Baltimo E||Instrument for ligating suturing and dividing organic tubular structures|
|US3765762 *||24 Sep 1971||16 Oct 1973||Donnici K Li||Copying machine|
|US4196836 *||14 Feb 1978||8 Apr 1980||Senco Products Inc.||Surgical stapling instrument|
|US4425915 *||26 Feb 1982||17 Jan 1984||Ethicon, Inc.||Surgical clip applier with in-line cartridge and interruptable biased feeder|
|US4595007 *||14 Mar 1983||17 Jun 1986||Ethicon, Inc.||Split ring type tissue fastener|
|US4664305 *||14 Jan 1985||12 May 1987||Blake Joseph W Iii||Surgical stapler|
|US4669469 *||28 Feb 1986||2 Jun 1987||Devices For Vascular Intervention||Single lumen atherectomy catheter device|
|US5100041 *||22 Nov 1989||31 Mar 1992||Technalytics, Inc.||Surgical stapler|
|US5158564 *||11 Jul 1990||27 Oct 1992||Angiomed Ag||Atherectomy apparatus|
|US5246156 *||12 Sep 1991||21 Sep 1993||Ethicon, Inc.||Multiple fire endoscopic stapling mechanism|
|US5346115 *||30 Mar 1992||13 Sep 1994||Eric Perouse||Surgical staple inserter|
|US5370651 *||10 Feb 1992||6 Dec 1994||Summers; David P.||Distal atherectomy catheter|
|US5392978 *||15 Oct 1993||28 Feb 1995||United States Surgical Corporation||Surgical staple and endoscopic stapler|
|US5431323 *||21 Jun 1993||11 Jul 1995||Ethicon, Inc.||Endoscopic surgical instrument with pivotable and rotatable staple cartridge|
|US5630540 *||24 May 1995||20 May 1997||United States Surgical Corporation||Surgical staple and staple drive member|
|US5695504 *||24 Feb 1995||9 Dec 1997||Heartport, Inc.||Devices and methods for performing a vascular anastomosis|
|US5720755 *||2 Oct 1995||24 Feb 1998||Dakov; Pepi||Tubular suturing device and methods of use|
|US5728047 *||27 Feb 1996||17 Mar 1998||Smc Surg-Med Devices, Inc.||Surgical instrument positioning system|
|US5829662 *||9 Sep 1996||3 Nov 1998||Ethicon, Inc.||Endoscopic surgical stapling instrument with pivotable and rotatable staple cartridge|
|US5908395 *||17 Mar 1997||1 Jun 1999||Advanced Cardiovascular Systems, Inc.||Vibrating guidewire|
|US5976159 *||8 Feb 1996||2 Nov 1999||Heartport, Inc.||Surgical clips and methods for tissue approximation|
|US6149660 *||22 Apr 1996||21 Nov 2000||Vnus Medical Technologies, Inc.||Method and apparatus for delivery of an appliance in a vessel|
|US6171330 *||15 Dec 1997||9 Jan 2001||Sofradim Production||Pneumatic surgical instrument for the distribution and placement of connecting or fastening means|
|US6450390 *||8 Jan 2001||17 Sep 2002||Hearport, Inc.||Surgical anastomosis apparatus and method thereof|
|US6592593 *||17 Sep 1999||15 Jul 2003||United States Surgical Corporation||Endovascular fastener applicator|
|US6830174 *||29 Aug 2001||14 Dec 2004||Cerebral Vascular Applications, Inc.||Medical instrument|
|US7309350 *||8 Aug 2003||18 Dec 2007||Xtent, Inc.||Apparatus and methods for deployment of vascular prostheses|
|US20020004663 *||7 May 2001||10 Jan 2002||Ventrica, Inc.||Methods and devices for placing a conduit in fluid communication with a target vessel|
|US20020108621 *||9 Apr 2002||15 Aug 2002||St. Jude Medical Cardiovascular Group, Inc.||Medical grafting methods and apparatus|
|US20030149441 *||23 Jan 2003||7 Aug 2003||Ruby Hill Ltd.||Method and apparatus for intraluminal fixation of intravascular devices|
|US20040176663 *||16 Dec 2003||9 Sep 2004||Edrich Vascular Devices, Inc.||Endovascular stapler|
|US20050004582 *||3 May 2004||6 Jan 2005||Edoga John K.||Endovascular stapler|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US7699203||13 Nov 2006||20 Apr 2010||Warsaw Orthopedic, Inc.||Variable angle surgical staple inserter|
|US7866524||21 Aug 2008||11 Jan 2011||Tyco Healthcare Group Lp||Stapler powered auxiliary device for injecting material between stapler jaws|
|US7975895||30 Apr 2010||12 Jul 2011||Tyco Healthcare Group L.P.||Tissue tensioner assembly and approximation mechanism for surgical stapling device|
|US7981124 *||4 Apr 2007||19 Jul 2011||Misder, Llc||Medical device for applying purse string sutures|
|US8011554||6 Jan 2009||6 Sep 2011||Tyco Healthcare Group, Lp||Raised boss for staple guide|
|US8146790||17 May 2010||3 Apr 2012||Tyco Healthcare Group Lp||Surgical instrument with safety mechanism|
|US8172121||2 Dec 2010||8 May 2012||Tyco Healthcare Group Lp||Stapler powered auxiliary device|
|US8181838||31 Aug 2009||22 May 2012||Tyco Healthcare Group Lp||Surgical stapling device|
|US8231042 *||20 Oct 2009||31 Jul 2012||Tyco Healthcare Group Lp||Surgical stapler|
|US8267301||21 Jun 2010||18 Sep 2012||Tyco Healthcare Group Lp||Surgical stapler|
|US8272555||7 Mar 2007||25 Sep 2012||Tyco Healthcare Group Lp||Stapler for mucosectomy|
|US8281974||7 Jan 2010||9 Oct 2012||Tyco Healthcare, Group LP||Surgical stapler with suture locator|
|US8317075||1 Aug 2011||27 Nov 2012||Covidien Lp||Raised boss for staple guide|
|US8322590||6 Oct 2010||4 Dec 2012||Covidien Lp||Surgical stapling instrument|
|US8343185||2 May 2012||1 Jan 2013||Covidien Lp||Surgical stapling device|
|US8348122||5 Sep 2006||8 Jan 2013||Tyco Healthcare Group Lp||Surgical stapling device|
|US8360295||21 May 2012||29 Jan 2013||Covidien Lp||Surgical stapling device|
|US8424535||5 Jul 2012||23 Apr 2013||Covidien Lp||Circular surgical stapler with mating anvil and shell assembly|
|US8430292||7 Oct 2010||30 Apr 2013||Covidien Lp||Surgical fastening apparatus|
|US8453911||18 Aug 2012||4 Jun 2013||Covidien Lp||Surgical stapler|
|US8453913||16 Jan 2010||4 Jun 2013||Covidien Lp||Anvil for surgical stapler|
|US8540132||16 May 2006||24 Sep 2013||Covidien Lp||Tilt anvil assembly|
|US8684248||29 Feb 2012||1 Apr 2014||Covidien Lp||Surgical instrument with safety mechanism|
|US8684251||24 Aug 2012||1 Apr 2014||Covidien Ag||Stapler for mucosectomy|
|US8684252||2 Nov 2012||1 Apr 2014||Covidien Lp||Surgical stapling instrument|
|US8701963 *||23 Feb 2011||22 Apr 2014||Dongguk University Industry-Academic Cooperation Foundation||Medical anastomosis apparatus|
|US8708212||18 Oct 2011||29 Apr 2014||Covidien Lp||Tilt top anvil with torsion spring|
|US8833630||14 Feb 2014||16 Sep 2014||Covidien Lp||Surgical instrument with safety mechanism|
|US8875974||21 Feb 2014||4 Nov 2014||Covidien Ag||Stapler for mucosectomy|
|US8893948||13 Mar 2014||25 Nov 2014||Covidien Lp||Tilt top anvil with torsion spring|
|US8905289||17 Feb 2014||9 Dec 2014||Covidien Lp||Surgical stapling instrument|
|US8931680||13 Aug 2014||13 Jan 2015||Covidien Lp||Surgical instrument with safety mechanism|
|US9010605||12 Jan 2012||21 Apr 2015||Covidien Lp||Sliding sleeve for circular stapling instrument reloads|
|US9016547||26 Oct 2011||28 Apr 2015||Covidien Lp||EEA tilt top anvil with ratchet/locking mechanism|
|US9022274||15 Feb 2012||5 May 2015||Covidien Lp||Circular stapler with increased lumen diameter|
|US9113871||18 Dec 2012||25 Aug 2015||Covidien Lp||Surgical stapling device|
|US9113886||27 Oct 2014||25 Aug 2015||Covidien Lp||Tilt top anvil with torsion spring|
|US9119621||29 Sep 2014||1 Sep 2015||Covidien Ag||Stapler for mucosectomy|
|US20060097025 *||6 Oct 2003||11 May 2006||Tyco Healthcare Graoup Llp||Surgical stapling device|
|US20070075117 *||5 Sep 2006||5 Apr 2007||Milliman Keith L||Surgical stapling device|
|US20100108741 *||20 Oct 2009||6 May 2010||Hessler Thomas R||Surgical stapler|
|EP1834593A1 *||16 Mar 2007||19 Sep 2007||Medtronic Vascular, Inc.||Prosthesis fixation apparatus and methods|
|International Classification||A61F2/06, A61B17/04, A61B17/115, A61B17/072, A61B17/12|
|Cooperative Classification||A61F2/06, A61B17/072, A61B17/12013, A61F2002/065, A61B2017/1157, A61B2017/1107, A61F2002/9517, A61B17/1155, A61B17/115, A61F2002/061|
|European Classification||A61B17/115, A61B17/072|
|14 Sep 2005||AS||Assignment|
Owner name: DATASCOPE INVESTMENT CORP., NEW JERSEY
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:FONTAYNE, DIEGO Y.;REEL/FRAME:016803/0819
Effective date: 20050816