The device comprises a prosthesis designed as a hollow body compressed against the action of restoring spring forces to a cross section reduced relative to an expanded use position, and held in this position by a strippable sheath. After the sheath is stripped, the prosthesis automatically expands to a cross section corresponding to the use position. The sheath, which can be a meshwork in the approximate form of crocheted material, extends over the entire length of the prosthesis and consists of at least one continuous thread and at least one drawstring. The prosthesis, held in the radially compressed position by the sheath, can be mounted displaceably on a feed wire or non-axially-displaceably on the insertion end of a probe or a catheter.
|
43. A system for implanting a prosthesis at a desired location in a body lumen, comprising:
a catheter constructed for percutaneous delivery, including a distal portion for receiving and carrying said prosthesis to said location, and a prosthesis release control mesh formed of a thread-like strand and surrounding said prosthesis for substantially its entire length, said release-control mesh being capable of maintaining said prosthesis on said catheter and said release control mesh further capable of being controllably unraveled from one end to the other by pulling an end of said thread-like strand to release said prosthesis from said catheter and allow it to be expanded into engagement with said body lumen at said desired site.
1. In combination, a device with a prosthesis implantable in a body of a patient, said prosthesis designed as a hollow body and being compressible against restoring spring forces to a cross section which is reduced relative to an expanded use position, said prosthesis also, after removal of restraining forces that maintain said prosthesis in reduced cross section, expanding automatically to a cross section that corresponds to the use position, wherein said device is a strippable sheath formed of at least one continuous thread surrounding said prosthesis in said reduced cross section, and at least one drawstring being layable to extend from the sheath that holds the prosthesis in reduced cross section, said drawstring being retractable to effect automatic expansion of said prosthesis by removing said sheath.
0. 52. In combination, a device with a prosthesis implantable in a body of a patient, said prosthesis designed as a hollow body and being compressible against restoring spring forces to a cross section which is reduced relative to an expanded use position, said prosthesis also, after removal of restraining forces that maintain said prosthesis in reduced cross section, expanding automatically to a cross section that corresponds to the use position, wherein said device comprises at least one strippable sheath formed of at least one continuous thread surrounding said prosthesis in said reduced cross section, and at least one drawstring extending from the sheath that holds the prosthesis in reduced cross section, said drawstring being retractable to effect automatic expansion of said prosthesis by removing said sheath.
2. The device according to
3. The device according to
4. The device according to
5. The device according to
6. The device according to
7. The device according to
8. The device according to
9. The device according to
10. The device according to
11. The device according to
12. The device according to
13. The device according to
14. The device according to
15. The device according to
16. The device according to
17. The device according to claim 1 52 wherein the prosthesis is a mesh tube including metal thread material.
18. The device according to
19. The device according to
21. The device according to
22. The device according to any one of claims 1 52, 2, 3, 5, or 17 wherein the sheath has successive mesh loops formed in opposite circumferential directions around the prosthesis, so that when successive mesh loops are stripped, the thread segments forming the loops come loose alternately on the right and left from the prosthesis.
23. The device according to
24. The device according to
25. The device according to
26. The device according to
27. The device according to any one of claims 1 52, 2, 3, 5, or 17 wherein the drawstring extends from a portion of the sheath surrounding a distal insertion end of the prosthesis so that when the sheath is stripped, the prosthesis gradually expands from the distal end to the proximal end.
28. The device according to claim 1 52 wherein an end of the thread forming the sheath is held by a strippable slipknot.
29. The device according to any one of claims 1 52, 3, or 17 wherein the sheath holding the prosthesis in its radially compressed position is formed of successive wrapping loops wrapped around the prosthesis at axial distances from one another, said wrapping loops being of a thread material extending along the inside of the prosthesis and pulled through a first hole in the prosthesis, the ends of said wrapping loops being guided back through a second hole in said prosthesis circumferentially adjacent to the first hole, and into the interior of the prosthesis, and said device further including a warp thread, running along the inside of the prosthesis and guided through the ends of the loops, the warp thread holding the loops in their wrapped positions.
30. The device according to any one of claims 1 52, 3, or 17 wherein the sheath holding the prosthesis in its radially compressed position is formed of wrapping loops wrapped around the prosthesis at axial distances from one another, said wrapping loops being of a thread material extending along the inside of the prosthesis and pulled through a first hole in the prosthesis, ends of said loops guided back into the interior of the prosthesis through a second hole spaced axially from the first hole, the wrapping loops being held in wrapping position by a loop formed from the thread material running inside the prosthesis being pulled through the end of the wrapping loop positioned inside the prosthesis, said loop passing through the end of the wrapping loop then extending outward through an adjacent hole in the axial direction and being wrapped around the prosthesis to form an adjacent wrapping loop.
31. The device according to claim 1 52 or 17 wherein the sheath is formed of shrinkable thread material.
32. The device according to claim 1 52 or 17 wherein the strippable sheath is includes a plurality of threads running parallel to one another.
33. The device according to claim 1 52 or 17 wherein at least two sheaths are provided wherein a first one of the two sheaths holds the prosthesis in the radially compressed state and a second sheath fits loosely around the prosthesis such that when the first sheath is stripped, the second sheath permits partial expansion of the prosthesis, said second sheath being subsequently strippable itself to permit full expansion.
34. The device according to claim 1 52 wherein the sheath is a meshwork surrounding the prosthesis with spaces between meshes filled and smoothed with a substance that dissolves in the body of a patient.
35. The device according to claim 1 52 wherein the thread material forming the sheath is provided with a lubricant to reduce friction.
36. The device according to claim 1 52 wherein at least the drawstring is constructed with metal so that it is visible in an x-ray image.
37. The device according to claim 1 52 wherein the proximal end of the prosthesis is flared in the expanded state, following removal of the sheath.
38. The device according to claim 1 52 or 17 wherein said prosthesis is formed by a patterned thread material.
41. The device according to claim 1 52 wherein said prosthesis is a mesh tube composed of plastic thread material.
42. The device of claim 1 52 or 35 wherein the thread forming said sheath is provided with a lubricant.
44. The system of
45. The system of
46. The system of
47. The system of
48. The system of claim 47 44 wherein the first loop is releasably secured to said catheter by an elastic sleeve attached to said catheter.
49. The system of
50. The system of any one of claims 43-49 wherein said mesh unravels from the distal end to the proximal end.
51. The system of any one of claims 43-49 wherein said prosthesis is a self-expanding prosthesis of the type that expands under spring force.
|
The invention relates to a device with a prosthesis implantable in the body of a patient, especially in a blood vessel or other body cavity, and designed as a hollow body. The prosthesis is compressible against the action of restoring spring forces down to a cross section which is reduced relative to an (expanded) operating position. The prosthesis may be also automatically expanding to a cross section corresponding to the operating position following removal of the restraining forces effecting the compression.
Devices of this type are known, and serve for percutaneous implantation of vascular prostheses in particular. Prostheses which are introducible percutaneously and expand in the lumen are either expandable mechanically by means of a known balloon catheter from a small radius to the larger radius to hold a vascular lumen open, or they expand automatically following previous compression prior to implantation by spring force, due to spring pretensioning generated during compression.
Various systems are already known for inserting self-expanding vascular prostheses which are under spring force into the body of a patient, and to implant or anchor them in the vessel by removing the restraining force.
The commonest method, which is described in EP-A-0 183 372, consists in compressing an endoprosthesis, made in the form of a tubular hollow body, to a reduced cross section and then pushing it in the compressed state, using a so-called pusher, through a catheter previously introduced into a vessel until they are in the correct position in the vessel. However, this system suffers from the disadvantage that a considerable expenditure of force is required to push the prosthesis through the catheter because its displacement is counteracted by considerable frictional forces.
Another method (not confirmable by publications) consists in retracting a sheath covering the endoprosthesis and holding the latter together, in the vessel at the implantation site. Here again there is the disadvantage that high frictional forces must be overcome. Moreover, the tube system is quite rigid because of the sheath covering the prosthesis, making introduction into a vessel through curves very difficult.
In another system (U.S. Pat. No. 4,732,152) a woven and spring-tensioned prosthesis is held together in the compressed state by a double sheath, sealed at the distal end. This sheath is retracted from the folded prosthesis like a stocking being pulled off the foot of a wearer. To reduce the friction which then occurs, liquid can be introduced between the two sheath layers. This system, which initially appears elegant because of the reduction of the frictional resistances, is extremely cumbersome to handle however and requires two persons to operate.
On the other hand, the invention is intended to provide an especially simple and readily operable device for implantation of a prosthesis made in the form of a hollow body, with a vascular prosthesis envisioned in particular.
This goal is achieved by virtue of the fact that in the device according to the preamble of claim 1 the prosthesis is surrounded by a sheath which can be pulled off it, said sheath consisting of at least one through thread, and compressed to a reduced cross section, and by the fact that at least one drawstring is provided, said drawstring being laid so it extends away from the sheath holding the prosthesis in its radially compressed state, the thread forming said sheath being retractable.
In the invention, the prosthesis is therefore held in its radially compressed state by means of this external sheath and reaches its intended expansion position only after removal of this sheath, which is designed to be pulled off, thanks to the pretensioning force generated during compression.
The sheath can be in particular a meshwork produced by crocheting, knotting, tying, or other methods of mesh formation.
Advantageously the prosthesis, held by the sheath which can be pulled off in the radially compressed state, can be received on a probe, or a flexible guide wire, and advanced thereon. In one design of a device of this kind, implantation is accomplished by introducing the guide wire in known fashion into a vessel and then advancing the prosthesis, held in a radially compressed state, along the guide wire, said wire being advanced for example by means of a sleeve likewise advanced over the guide wire and engaging the end of the prosthesis away from the insertion end thereof.
Another improvement, on the other hand, provides that the prosthesis, held in the radially compressed state by the sheath which can be pulled off, is held in an axially fixed position on the insertion end of a probe. Specifically, this probe can be a catheter advanced over a guide wire.
Even with the axially fixed mounting of the prosthesis, held in the compressed state, on the insertion end of a probe or a catheter, implantation takes place in simple fashion with the probe or catheter being advanced together with the prosthesis mounted on the insertion end, for example under the control of x-rays, up to the implantation site, and then by pulling off the sheath, made for example as a covering meshwork, the prosthesis is exposed and implanted in the proper location by its automatic expansion.
In mounting the prostheses on the insertion ends of probes or catheters, it has been found to be advantageous for the prosthesis to be mounted on a non-slip substrate surrounding the probe or catheter, so that undesired slipping and sliding during the release of the thread material forming the meshwork cannot occur.
Advantageously, the self-expanding prosthesis can be a tube made by crocheting, knitting, or other methods of mesh formation, composed of metal and plastic thread material with good tissue compatibility, said tube being compressible radially against the action of pretensioning forces and automatically expanding into its operating position after the restraining forces are removed, and then remaining in the expanded position.
In the case of the prosthesis designed as meshwork, according to a logical improvement, successive rows of mesh can be made alternately of resorbable thread material and non-resorbable thread material. This means that within a predetermined period of time after implantation, the resorbable thread material will be dissolved and the prosthesis parts, then consisting only of non-resorbable thread material, will remain in the patient's body. These remaining components form circumferential rings of successive open loops. This avoids thread intersections which could exert undesirable shearing forces on surrounding and growing tissue coatings.
In the improvement just described, drugs can also be embedded in the resorbable thread material so that the prosthesis constitutes a drug deposit which gradually dispenses drugs during the gradual dissolution of the resorbable thread material.
An especially advantageous improvement on the invention is characterized by making the tubular meshwork holding the prosthesis in the compressed state in such a way that the mesh changes direction after each wrap around the prosthesis and when successive meshes are pulled off, the thread sections forming the latter separate alternately to the right and left from the prosthesis.
The advantage of this improvement consists in the fact that the mesh wrapped successively and alternately left and right around the prosthesis can be pulled off without the thread material becoming wrapped around the probe holding the prosthesis or a catheter serving as such, or undergoing twisting, which would make further retraction of the thread material more difficult because of the resultant friction.
It has also been found to be advantageous in the improvement described above for the loops or knots of the mesh wrapped successively around the prosthesis and capable of being pulled off, to be located sequentially with respect to one another or in a row running essentially axially.
Another important improvement on the invention provides for the drawstring to extend away from the mesh surrounding the insertion end of the prosthesis, and therefore the prosthesis, as the meshwork is pulled off its distal end, gradually reaches its expanded position.
In this improvement, the thread material to be pulled off when the prosthesis is tightened can never enter the area between the already expanded part of the prosthesis and the wall of a vessel for example. The thread material to be pulled off instead extends only along the part of the mesh which has not yet been pulled off and thus in the area of the prosthesis which is still held in the compressed position.
The ends of the thread material forming the meshwork can be held by releasable knots, in the form of so-called slip knots for example, and thereby have their releasability preserved. One especially simple means that has been found for axial mounting of the prosthesis on a probe or on a catheter serving as such is for the beginning of the thread material forming the meshwork and an end mesh to be pinched in holes in the probe or catheter, yet capable of being pulled out of their pinched positions by means of the drawstring. The beginning of the thread material can be pinched between the probe and the cuff mounted held on the latter, however.
The cuff material is held especially securely, but at the same time in such a way that it can be easily pulled off, if from the knot of the mesh of the first mesh on the pull-off side of the meshwork, a loop passed through a hole extends, one end of said loop making a transition in the vicinity of the above knot to the drawstring. As a result, this loop can be pulled off by means of the drawstring through the above-mentioned knot and then all of the mesh forming the meshwork can be pulled off in succession.
According to another logical improvement on the invention, the prosthesis can also be held in its radially compressed position by means of a meshwork applied from the distal end of the probe or catheter and extending over the insertion end of the prosthesis and by means of a meshwork that extends in the direction opposite the proximal end and also extends over the end mesh of the first meshwork. It has been found advantageous in this connection for the two meshworks to be capable of being pulled off in opposite directions from their loop-shaped end meshes by means of drawstrings.
In a design of this kind, following correct placement of the prosthesis mounted on a probe or a catheter in a vessel, the meshwork applied from the distal end is pulled off first, beginning with the end mesh removed from the distal end and then advancing gradually until this meshwork is removed completely and the thread material is retracted. Then the meshwork applied from the proximal end is pulled off, starting with the end mesh toward the distal end and then advancing toward the proximal end. It is obvious that when the meshwork is pulled off in this way, the self-expanding prosthesis is expanded gradually, starting at its distal end, into its intended operating position.
In another important embodiment, the sheath that holds the prosthesis in its radially compressed position consists of loops surrounding the prosthesis and spaced axially apart, said loops being formed by the thread material, pulled through a hole in the prosthesis, of a thread guided along inside the prosthesis, with the ends of the loops each being brought back through a hole, adjacent to the first hole in the circumferential direction, into the interior of the prosthesis, and a warp thread, likewise running along the inside of the prosthesis and guided through the ends of the loops, holds in the loops in their wrapping positions. It is clear that in this design the prosthesis is released by pulling the warp thread out of the end segments of the loops, and that the thread material forming the loops, like the warp thread, can be retracted in simple fashion. In a similar improvement on the invention, the sheath holding the prosthesis in its radially compressed position consists of loops which are axially spaced apart and are wrapped around the prosthesis, said loops being formed by thread material, pulled through a hole in the prosthesis, of a thread guided along inside the prosthesis, with the ends of the loops each being brought back into the interior of the prosthesis through holes spaced axially from the first hole, and held in place by the fact that a loop formed from the thread material running inside the prosthesis is pulled through each loop end brought back into the prosthesis, said loop then being brought out through a hole following in the axial direction, then being wrapped around the prosthesis and brought back in the same manner with its loop end passing through a hole into the prosthesis and being secured in this position. In this design also, the pulling off of the sheath holding the prosthesis in its radially compressed position is accomplished in simple fashion by means of the thread extending from the last loop, from which the loops surrounding the prosthesis are formed.
For especially tight wrapping and the resultant compression of the prosthesis, it has also been found advantageous to use shrinkable thread material to form the meshwork. The meshwork that can be pulled off can also consist of a plurality of threads running parallel to one another.
Another important improvement on the invention provides that between the prosthesis and the sheath holding the latter in the radially compressed state, at least one additional sheath is provided which loosely fits around the prosthesis and allows a partial expansion of the prosthesis when the outer sheath is pulled off, and is itself subsequently capable of being pulled off.
This improvement is also one that involves a sheath, surrounding the prosthesis loosely and with a certain amount of play, being mounted on said prosthesis, which can be a meshwork, with the prosthesis and the inner sheath being surrounded closely by an outer sheath which holds the prosthesis, together with the sheath mounted directly on it, in the radially compressed state. The prosthesis is consequently surrounded by two layers, so to speak, and after the outer sheath is stripped, can expand only within the limits set by the inner sheath. The final implantation is then accomplished by stripping the inner sheath, i.e. in stages.
Of course, several meshworks surrounding one another with a certain amount of play can be provided, which permit expansion of the prosthesis in several successive stages.
Within the scope of the invention, the spaces between the meshes of a meshwork surrounding the prosthesis and holding it in the compressed state can be filled and smoothed with gelatin or a similar substance which dissolves in the body of a patient. This facilitates introduction of such a device.
According to yet another improvement, at least one end of the prosthesis can be surrounded in the compressed state by a cuff, said end, because of the axial shortening of the prosthesis that takes place during expansion, escaping the grip exerted by the cuff. A cuff of this kind can be mounted permanently on the probe and/or a catheter, with the open side facing the prosthesis, for example on the side toward the distal end. This produces a smooth transition that facilitates introduction, at the end of the prosthesis which is at the front in the insertion device.
For improved attachment of the prosthesis to a probe or to a catheter serving as same, the end of the prosthesis facing away from the insertion end can abut at a radially projecting step or shoulder or a cuff mounted on the probe or catheter.
Yet another improvement on the invention provides that when a catheter is used as a probe, the drawstring is introduced through a hole passing through the catheter wall in the vicinity of one end of the prosthesis, enters the lumen of the catheter, extends through the latter, and extends beyond the end of the catheter.
However, a double-lumen catheter can also serve as a probe with one lumen serving to advance the catheter over a guide wire and the other lumen being used to guide the drawstring.
When using a catheter with one or two lumina as a probe, with the drawstring passing through the catheter lumen, assurance is provided that the walls of the vessels or other body cavities in which a prosthesis is to be implanted cannot be damaged by the drawstring and/or, when the meshwork is stripped, by the thread material, which is then pulled back through the catheter lumen.
It has also proven to be advantageous for the drawstring and/or the thread material of the meshwork to be provided with a friction-reducing lubricant.
In addition, at least the drawstring can be made in the form of a metal thread or provided with an admixture of metal, so that good visibility with x-rays is ensured.
Finally, according to yet another improvement, the prosthesis, kept in the radially compressed position by the strippable sheath, can expand to resemble a trumpet at its proximal end in the expanded state following removal of the sheath,. This prosthesis design is important for implants in the vicinity of branches in the vessels, because there is always the danger of the prosthesis slipping into the branching vessel. In view of the trumpet-shaped expansion at the proximal end, however, such slipping during implantation is effectively suppressed when the sheath surrounding the prosthesis is stripped off the proximal end.
One embodiment of the device according to the invention will now be described with reference to the attached drawing. Schematic views show the following:
In device 10 shown in
Prosthesis 15 is surrounded by a crocheted material 14 formed by a continuous thread, with successive meshes wrapped around the prosthesis alternately on one side or the other, in other words alternately on the right or left side. The initial section 17 of the thread material, located in front of the first mesh 16 associated with the distal end 12 of catheter 11, is pulled through a slot 18 in the catheter wall, pinched in said slot, and then extends through the catheter lumen and out through the distal end of the catheter. A strippable loop 22 is pulled through a knot 21 that closes end mesh 20 which is remote from the distal end, said loop being pulled through two cuts 23, 23' in the catheter wall, and is therefore likewise held axially by pinching.
The free thread end guided through knots 21 of said end mesh 20 forms a drawstring 24 extending along catheter 11, by means of which drawstring, first loop 22 held on the catheter by pinching and then gradually the mesh formed of crocheted material extending around the prosthesis and holding the latter in its compressed state, can be stripped through said end knot. Since the meshes are wrapped alternately right and left around prosthesis 15, when the mesh is stripped the threads on the right and left sides of the catheter are released alternately from the corresponding mesh knots, and after the mesh facing the distal end comes loose, initial segment 17 of the thread material can be pulled out of its pinched position in slot 18 at distal end 12 of catheter 11.
In an enlarged view,
To form the next mesh, as shown in
Loop 22, pulled through the loop associated therewith or through a knot 21 formed by pulling together these loops to form end mesh 20, is then pulled in the manner shown schematically in FIG. 1 through the two axially spaced slots 23, 23' in the wall of the catheter and held in place by pinching. The remaining thread material then forms drawstring 24 which extends from the loop of end mesh 20 and permits the crocheted material to be stripped, with the thread material of the meshes as they are stripped alternately coming loose on one side or the other of prosthesis 15, thereby releasing the prosthesis to expand under the pretensioning force imposed during crocheting as a result of radial compression.
In embodiment 40 shown in
The crocheted material that holds prosthesis 45 in the compressed position shown in
The prosthesis 45 in the embodiment shown in
Since the end of the prosthesis that points toward the distal catheter end is released by stripping crocheted material 46 applied from the distal end, this end of the prosthesis expands radially as a result of the pretensioning forces of the prosthesis itself, while the remaining part of the prosthesis is still held in the compressed position by crocheted material 47 applied from the proximal end. Partially expanded prosthesis 45 is axially immobilized in this position both by the adhesive effect between the catheter and the prosthesis and by a silicone cuff 62 mounted on the proximal end of prosthesis 45 on catheter 41, which cuff the prosthesis abuts axially.
After stripping first crocheted material 46, crocheted material 47 applied from the proximal end is also stripped, specifically by means of drawstring 60 extending from its end mesh 58 on the side pointing toward the distal end. It is clear that when the drawstring is pulled, loop 58 held at the distal end beneath silicone cuff 43 is stripped first and then meshes 57 and 56 are stripped, starting at the side facing the distal end, gradually in the direction of the proximal end, with prosthesis 45 expanding radially and abutting the walls of a vessel to be equipped with a prosthesis. At the end of the stripping process, thread end 55 located beneath silicone cuff 54 at the proximal end is pulled free. Prosthesis 45 is then free of catheter 41 and the latter can be withdrawn in simple fashion out of the vessel.
Prosthesis 70 shown in
The advantage of the embodiment shown in
The prosthesis according to
The embodiment shown in
Referring to
The advantage of this prosthesis design consists in the fact that the resorbable thread material dissolves following expiration of a predetermined period of time after implantation, and then only the non-degradable components remain in the body of a patient. These remaining components form circular rings of successive open loops. In this manner, thread crossings are avoided, which could exert unnecessary shearing forces on the surrounding and growing tissue coatings.
Prostheses according to
Patent | Priority | Assignee | Title |
10016274, | Jan 24 2008 | Medtronic, Inc. | Stent for prosthetic heart valves |
10646335, | Jan 24 2008 | Medtronic, Inc. | Stents for prosthetic heart valves |
10758343, | Jan 24 2008 | Medtronic, Inc. | Stent for prosthetic heart valves |
10820993, | Jan 24 2008 | Medtronic, Inc. | Stents for prosthetic heart valves |
11083573, | Jan 24 2008 | Medtronic, Inc. | Delivery systems and methods of implantation for prosthetic heart valves |
11259919, | Jan 24 2008 | Medtronic, Inc. | Stents for prosthetic heart valves |
11284999, | Jan 24 2008 | Medtronic, Inc. | Stents for prosthetic heart valves |
11607311, | Jan 24 2008 | Medtronic, Inc. | Stents for prosthetic heart valves |
11786367, | Jan 24 2008 | Medtronic, Inc. | Stents for prosthetic heart valves |
6878161, | Jan 05 1996 | HYPERION MATERIALS & TECHNOLOGIES SWEDEN AB | Stent graft loading and deployment device and method |
6984242, | Dec 20 2002 | W L GORE & ASSOCIATES, INC | Implantable medical device assembly |
7320703, | Jun 21 2002 | LifeShield Sciences LLC | Method for inserting a prosthesis |
7753907, | Oct 29 2004 | Boston Scientific Scimed, Inc | Medical device systems and methods |
7927363, | Dec 02 2005 | W L GORE & ASSOCIATES, INC | Device for treating a blood vessel and associated treatment kit |
8157852, | Jan 24 2008 | Medtronic, Inc | Delivery systems and methods of implantation for prosthetic heart valves |
8157853, | Jan 24 2008 | Medtronic, Inc | Delivery systems and methods of implantation for prosthetic heart valves |
8226710, | May 13 2005 | Medtronic CoreValve, Inc. | Heart valve prosthesis and methods of manufacture and use |
8303616, | Sep 10 2001 | Boston Scientific Scimed, Inc. | Internal restraint for delivery of self-expanding stents |
8673000, | Jan 24 2008 | Medtronic, Inc. | Stents for prosthetic heart valves |
8685077, | Jan 24 2008 | Medtronics, Inc. | Delivery systems and methods of implantation for prosthetic heart valves |
9060857, | May 13 2005 | Medtronic Corevalve LLC | Heart valve prosthesis and methods of manufacture and use |
9149358, | Jan 24 2008 | Medtronic, Inc | Delivery systems for prosthetic heart valves |
9339382, | Jan 24 2008 | Medtronic, Inc. | Stents for prosthetic heart valves |
9433502, | Nov 27 2009 | VENUS MEDTECH HANGZHOU , INC | Apparatus and set for folding or unfolding a medical implant and method |
Patent | Priority | Assignee | Title |
4629459, | Dec 28 1983 | SORIN BIOMEDICAL INC | Alternate stent covering for tissue valves |
4732152, | Dec 05 1984 | AMS MEDINVENT S A | Device for implantation and a method of implantation in a vessel using such device |
4878906, | Mar 25 1986 | Servetus Partnership | Endoprosthesis for repairing a damaged vessel |
4913141, | Oct 25 1988 | Cordis Corporation | Apparatus and method for placement of a stent within a subject vessel |
4922905, | May 28 1987 | Boston Scientific Corporation | Dilatation catheter |
5147400, | May 10 1989 | United States Surgical Corporation | Connective tissue prosthesis |
5234456, | Feb 08 1990 | SciMed Life Systems, INC; Boston Scientific Scimed, Inc | Hydrophilic stent |
5234457, | Oct 09 1991 | Boston Scientific Scimed, Inc | Impregnated stent |
5653748, | May 20 1992 | Boston Scientific Scimed, Inc | Device with a prosthesis implantable in the body of a patient |
DE35424753, | |||
DE3640745, | |||
DE4037507, | |||
DE40375072, | |||
DE4137857, | |||
EP183372, | |||
EP292587, | |||
EP382014, | |||
FR2333487, | |||
GB1173811, | |||
GB1565828, | |||
WO9102194, |
Executed on | Assignor | Assignee | Conveyance | Frame | Reel | Doc |
Apr 10 1997 | Boston Scientific Corporation | (assignment on the face of the patent) | / |
Date | Maintenance Fee Events |
Sep 26 2006 | M1553: Payment of Maintenance Fee, 12th Year, Large Entity. |
Date | Maintenance Schedule |
Apr 22 2006 | 4 years fee payment window open |
Oct 22 2006 | 6 months grace period start (w surcharge) |
Apr 22 2007 | patent expiry (for year 4) |
Apr 22 2009 | 2 years to revive unintentionally abandoned end. (for year 4) |
Apr 22 2010 | 8 years fee payment window open |
Oct 22 2010 | 6 months grace period start (w surcharge) |
Apr 22 2011 | patent expiry (for year 8) |
Apr 22 2013 | 2 years to revive unintentionally abandoned end. (for year 8) |
Apr 22 2014 | 12 years fee payment window open |
Oct 22 2014 | 6 months grace period start (w surcharge) |
Apr 22 2015 | patent expiry (for year 12) |
Apr 22 2017 | 2 years to revive unintentionally abandoned end. (for year 12) |