Device for fastening and anchoring cardiac valve prostheses

Information

  • Patent Grant
  • RE45130
  • Patent Number
    RE45,130
  • Date Filed
    Thursday, June 26, 2008
    16 years ago
  • Date Issued
    Tuesday, September 9, 2014
    10 years ago
  • US Classifications
    Field of Search
    • US
    • 623 00211-00219
    • 623 001240
    • 623 001260
    • 623 900000
    • 623 001150
  • International Classifications
    • A61F2/24
    • A61F2/06
Abstract
This invention relates to a device for fastening and anchoring heart valve prostheses which is essentially formed of wire-shaped interconnected elements. The aim of the invention is to be able to be implant, in a minimally invasive manner, a device of this type via the aorta by compressing the device to make it smaller, and by extending the same at the site of implantation, whereby ensuring a secure retention and a secure sealing with regard to the aorta wall. To this end, the invention provides that for fastening and supporting a cardiac valve prosthesis, three identical pairs of arched elements are interconnected, with a configuration that is offset by 120°, by means of solid body articulations. These solid body articulations carry out the function of pivot bearings.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a U.S. national counterpart application of international application serial no. PCT/DE01/00837 filed Feb. 28, 2001, which claims priority to German application serial No. 100 10 074.0 filed Feb. 28, 2000.


BACKGROUND AND SUMMARY OF THE INVENTION

The invention relates to a device for fastening and anchoring cardiac valve prostheses which is essentially formed of wire-shaped interconnected elements. In the folded up state it is allowed to be introduced through the aorta in a minimally invasive manner, and be anchored in the aorta wall after being deployed such that the implanted and secured heart valve prosthesis is allowed to adopt the function of the endogenous heart valve.


Heretofore, it did not succeed in a satisfactory extent to suggest a solution wherein both a secure sealing against the aorta wall and a secure retention can be ensured. On that occasion, such a device or such an anchoring support (stent) must be able to be folded up small enough in order to be stretched then at the site of implantation. With the known solutions a satisfactory enlargement will not be achieved with the appropriate tension force which is allowed to ensure such a retention. Proposals in which a form storage metal (memory metal) is to be used as well do not meet the requirements although an expansion takes place with these materials when a transition temperature has been reached and exceeded, respectively.


The solution as described in U.S. Pat. No. 5,411,552 cannot meet the requirements as well since a relatively instable object is to be used.


Another problem which is solved in an unsatisfactory manner so far is the secure attachment of an artificial or biological heart valve prosthesis. As a rule, the prostheses are lavishly sewn on to a stent. This is time-consuming and has to be carried out with great care in order to avoid damages.


Since the implanted heart valve prostheses have to be able to function over long periods the constructional design plays an essential role as well since damages and leakages can occur after the implantation otherwise which can result in life threatening states of the patient.


Hence, it is an object of the invention to suggest a device for fastening and anchoring heart valve prostheses which can be folded up small enough, and deployed at the site of implantation for a minimally invasive implantation through the aorta wherein a secure retention and a secure sealing with respect to the aorta wall are ensured.


According to the invention this object is solved with a device according to claim 1.


Advantageous embodiments and improvements of the invention can be achieved with the features mentioned in the subclaims.


Three identical pairs of arched elements each are substantial elements of the solution according to the invention which are interconnected in a configuration that is offset by 120°. The two arched elements of one pair are bent opposite to each other in a curved manner and connected by means of solid articulations. The solid articulations simultaneously meet the function of pivot bearings about which the arched elements of one pair can be swivelled similarly as with a seesaw. If a pressure force is exerted upon one of the arched elements, e.g. through the peristaltic action of the aorta, this arched element will be swivelled according to the same direction about the axis of rotation on the solid articulation. Simultaneously, the respective other arched element of the pair will be swivelled opposite thereto. Therefore, one of the two arched elements of the pair is then already pressed against the aorta wall increasing the sealing and the retention.


It is favourable to dimension the arched elements of a pair such that as far as possible the same lever relations are met with respect to the solid articulations forming the pivot bearings, thus rocker arms with an identical length or at least with approximately the same length will be formed.


The relative great distances of the solid articulations predetermined by the configuration of 120° of the pairs of arched elements, and the large surface areas covered by the arched elements as well are also advantageous wherein the distal arched elements do not only serve for fastening the heart valve prosthesis but also adopt a supporting function.


The mentioned advantages can still be improved by means of another curved arched element which is arranged in the distal direction.


On that occasion, the second distal arched element in its distal area is designed in a curved manner approximately like the first distal arched element. Partly, these two arched elements are designed and shaped such that they pass adjacent to each other, and gaps are formed between them. They are allowed to be interconnected at the same place at which the solid articulations are also arranged as a connection toward the arched element curved in the proximal direction. Hence, the formed gaps are open in the distal direction, and portions of the heart valve prosthesis are allowed to be introduced into the gaps and be supported.


At least one portion of a distal arched element is proximally retracted and guided up to a turning point in which adjacent arched elements are collected. With two distally arranged arched elements this applies to the respective distally outer arched element.


For stiffening and as a further possibility of fastening the heart valve prosthesis it is allowed to use an angular curved arched element being proximally retracted as well, the curved portions of which are located between the respective adjacent arched elements and are formed partly following the respective curvature. These arched elements with the distal ends thereof are secured to the one distally outer arched element or the respective distally outer arched element. Herein, the attachment also forms a respective solid articulation. These should still be located in a distance to the other solid articulations connecting one pair.


With a device being implanted and stretched over the pockets of a heart valve prosthesis then can be pushed in, held and supported there.


The construction of the arched element of the device according to the invention supports a heart valve prosthesis in a large-surface manner, and therefore with care. Additionally, it is allowed to be fastened with a substantially lower amount, for example by sewing.


The constructional solution enables a secure retention and the required sealing on the aorta wall, and with respect thereto, respectively. Pressing against the heart valve prosthesis from the inside by means of the arched element is advantageous for the sealing and for a reduced load of the heart valve prosthesis.


The device according to the invention can be implanted by means of a balloon catheter and can be deployed at the site of implatation. Advantageously, for the device is used a form storage metal as well having a suitable transition temperature by means of which an extension can be additionally achieved. For this, an alloy containing nickel and titanium can be employed which is available under the designation of Nitinol.


Moreover, the portion of the device supporting and holding the heart valve prosthesis can be implanted separately to a supporting body which is still referred to hereinafter with the description of an embodiment without reducing the advantageous properties. The implantation of this portion substantially consisting of the three segments having the heart valve prosthesis attached thereto then can operatively take place in a conventional form.


In the text that follows, the invention will be explained in more detail according to an embodiment in which





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 shows a developed view of an embodiment of a device according to the invention.





DETAILED DESCRIPTION OF THE DRAWINGS

In FIG. 1 is shown a developed view of an embodiment of a device according to the invention. The device is radially symmetrically designed wherein three identical portions are used in a configuration of 120°.


Each portion uses an arched element construction as a carrier and for fastening an artificial or biological heart valve prosthesis.


With this embodiment two arched elements 4 and 5 are used which are distally arranged outside wherein the outer arched element 5 could be abandoned as the case may be.


The arched element 4 bent into a curved manner is connected to an arched element 3 which is bent in the opposite direction. The two sided connections represent solid articulations 7 which simultaneously adopt pivot functions for the two arched elements 3 and 4 representing levers as it is already described in the general part of the description.


The second arched element 3 which is outwardly bent and distally arranged increases the stability and offers an additional supporting and fastening possibility for the heart valve prosthesis. On that occasion, the two distally outer arched elements 4 and 5 are interconnected as well, wherein this connection is allowed to occur at the same place at which the solid articulations 7 are also arranged.


There are gaps between the two arched elements 4 and 5 which are open from the distal direction into which the portions of the heart valve prosthesis can be introduced and fixed there.


The arched element 5 being the outer one here is further inwardly pulled in the proximal direction, and is connected with its end to a respective supporting ridge 8. In this embodiment, the supporting ridges 8 are aligned in parallel to the longitudinal axis of the device, and together with saw tooth shaped, rhombic or meander shaped transversal ridges they form a supporting body which in the deployed state closely fits on the aorta wall. For interlocking, additional tips 9 can be present and designed, respectively, on the supporting ridges 8, and/or the transversal ridges which interlock in the aorta wall.


The configuration and length of the supporting ridges 8, and the respective great distance toward the heart valve prosthesis fastened in the area of the arched elements 3, 4 and 5 enable positioning the heart valve prosthesis without locking and covering the coronary vessels, respectively.


With the embodiment as shown herein, additional arched elements 2 being proximally pulled in are present between the individual segments used in a configuration of 120° which are connected to the distally outer arched elements 5. Herein, the connections are solid articulations 6 as well, however, which should be arranged in a distance toward the solid articulations 7 as far as possible. Thus, two levers per segment can be used, and forces twice as large can be realized with such a double-reflected structure in order to fix the device.


In the deployed implanted state the portions of the heart valve prosthesis can be mutually introduced in turn between the portions 1 of the arched elements 5 and the arched elements 2, thus being supported and fixed thereto.


The number of the arched elements used can still be increased, however, to improve the retention and to further decrease the load of the heart valve prosthesis.

Claims
  • 1. A device for fastening and anchoring a heart valve prosthesis, the device consisting of three identical sections, each section being coupled to adjacent sections on each side of said section by an elongated supporting ridge extending in a direction generally parallel to a longitudinal axis of the device, each section having a first arched element arched in a first direction, a second arched element arched in the first direction, and a third arched element arched in a second direction opposite from the first direction, the second and third arched elements being coupled to the first arched element at first points to define between the first and second arched elements a first space, each section further comprising a fourth arched element arched in the second direction and having ends coupled to the first arched element of said section and athe first arched element of an adjacent section at second points distinct from the first points to define between the fourth arched element and the adjacent first arched elements a second space.
  • 2. A device for supporting a heart valve prosthesis, the device consisting essentially of three substantially identical elements, each element being coupled to adjacent elements on each side of said element by an elongated supporting member extending in a direction generally parallel to a longitudinal axis of the device, each element including a first arched member coupled to, and extending in a first direction generally away from said first arched member's respective supporting members, and a second arched member coupled to the first arched member at points different from the first arched member's coupling to its respective supporting members, the second arched member extending generally in a second direction opposite from the first direction, wherein each element further includes a third arched member coupled to the first arched member at substantially the same points as the second arched member is coupled to the first arched member, the third arched member extending generally in the first direction, each element further including a pair of fourth arched members, each of said fourth arched members extending alongside, and conforming generally to, the curvature of a portion of the first arched member, each of the fourth arched members being coupled to a first arched member intermediate opposite ends of said first arched member and extending from said coupling to said first arched member generally in said second direction toward a respective supporting member.
  • 3. The device of claim 2 wherein each fourth arched member extends to a point adjacent a respective supporting member, turns, and extends generally in the first direction, conforming generally to the curvature of a portion of a first arched member of an adjacent element on one side of said element.
  • 4. The device of claim 3 wherein each element further includes transversal members extending between its respective supporting members.
  • 5. The device of claim 4 wherein at least some of said transversal members include tips to facilitate anchoring of said device into tissue of a vessel or the heart of a wearer of the device.
  • 6. The device of claim 4 constructed from memory metal.
  • 7. The device of claim 3 constructed from memory metal.
  • 8. The device of claim 2 wherein each element further includes transversal members extending between its respective supporting members.
  • 9. The device of claim 8 wherein at least some of said transversal members include tips to facilitate anchoring of said device into tissue of a vessel or the heart of a wearer of the device.
  • 10. The device of claim 8 constructed from memory metal.
  • 11. The device of claim 2 constructed from memory metal.
  • 12. A medical device, in combination with a heart valve prosthesis, the medical device consisting of three substantially identical sections, each section being coupled to adjacent sections on each side of the section, the medical device being implantable in a body via a catheter and including a collapsed mode and an expanded mode, each section including: a first arched element arched in a first direction, the first arched element disposed at a distal end of the device;a second arched element arched in the first direction, the second arched element disposed at the distal end of the device and connected to the first arched element at first points; anda fourth arched element arched in a second direction opposite from the first direction and having ends coupled to the first arched element of said section and the first arched element of an adjacent section at second points distinct from the first points to define between the fourth arched element and the adjacent first arched elements a space;wherein the heart valve prosthesis is fixedly attached to the first, second, and fourth arched elements of each of the three sections and remains fixedly attached to function as a heart valve after removal of the catheter from the body, the heart valve prosthesis repeatedly opening and closing to allow and prevent blood flow, respectively, through the medical device.
  • 13. The medical device, in combination with the heart valve prosthesis of claim 12, each section further including: a third arched element arched in the second direction, the third arched element connected to the first and second arched elements at the first points.
  • 14. The medical device, in combination with the heart valve prosthesis of claim 13, wherein each section further includes an eyelet element disposed at a proximal end of the device opposite the distal end.
  • 15. The medical device, in combination with the heart valve prosthesis of claim 12, wherein each of the three fourth arched elements conforms generally to a curvature of a portion of the first arched element of the first section and the curvature of a portion of the first arched element of the adjacent section.
  • 16. The medical device, in combination with the heart valve prosthesis of claim 12, wherein at least one of the second points pivots when a pressure force is exerted upon one of the first or fourth arched elements.
  • 17. The medical device, in combination with the heart valve prosthesis of claim 12, wherein the device is configured to be implanted within an aorta.
  • 18. The medical device, in combination with the heart valve prosthesis of claim 12, wherein each section is coupled to the adjacent sections by a supporting ridge, each section further including transversal members extending between adjacent elongated supporting ridges.
  • 19. The medical device, in combination with the heart valve prosthesis of claim 18, wherein at least some of said transversal members include tips to facilitate anchoring of said device into tissue of a vessel or a heart of a patient.
  • 20. The medical device, in combination with the heart valve prosthesis of claim 18, wherein the transversal members have a saw-tooth shape.
  • 21. The medical device, in combination with the heart valve prosthesis of claim 18, wherein the transversal members have a rhombic shape.
  • 22. The medical device, in combination with the heart valve prosthesis of claim 12, wherein the heart valve prosthesis is a biological heart valve prosthesis.
  • 23. The medical device, in combination with the heart valve prosthesis of claim 12, wherein the heart valve prosthesis is an artificial heart valve prosthesis.
  • 24. The medical device, in combination with the heart valve prosthesis of claim 12, wherein the three sections are spaced substantially 120 degrees apart.
  • 25. The medical device, in combination with the heart valve prosthesis of claim 12, wherein the device is constructed from memory metal.
  • 26. The medical device, in combination with the heart valve prosthesis of claim 12, wherein the device is balloon expandable.
  • 27. A medical device, in combination with a heart valve prosthesis, the medical device consisting of three substantially identical sections, each section being coupled to adjacent sections on each side of the section, the medical device being implantable in a body via a catheter and having a first, compressed mode and a second, expanded mode, each section including: a first arched element arched in a first direction, the first arched element disposed at a distal end of the device;a third arched element arched in a second direction opposite from the first direction, the first and third arched elements connected to each other at a first point, wherein between an apex of the first arched element and an apex of the third arched element there is a space; anda fourth arched element arched in a direction opposite from the first direction and having a first end coupled to the first arched element of said section at a second point and a second end coupled to the first arched element of an adjacent section at a third point, the second point and the third point being distinct from the first point to define between the fourth arched element and the adjacent first arched elements a space;wherein the heart valve prosthesis is fixedly attached to the first and fourth arched elements of each of the three sections and remains fixedly attached to function as a heart valve after removal of the catheter from the body, the heart valve prosthesis repeatedly opening and closing to allow and prevent blood flow, respectively, through the medical device.
  • 28. The medical device, in combination with the heart valve prosthesis of claim 27, wherein the first point is a pivot point about which the third arched element can move.
  • 29. A medical device, in combination with a heart valve prosthesis fixedly attached to the medical device, the medical device consisting of three substantially identical sections, each section being coupled to adjacent sections on each side of the section, the medical device being implantable in a body via a catheter and having a first, compressed mode and a second, expanded mode, each section including: a first arched element arched in a first direction, the first arched element connected to a supporting ridge and disposed on a first, distal end of the supporting ridge;a third arched element arched in a second direction opposite from the first direction, the first and third arched elements connected to each other at a first point, wherein between an apex of the first arched element and an apex of the third arched element there is a space; anda fourth arched element arched in a direction opposite from the first direction and having ends coupled to the first arched element of said section and the first arched element of an adjacent section, wherein a curvature of the fourth arched element is different from a curvature of the third arched element; anda plurality of undulating transverse ridges connected to the supporting ridge and disposed on a second, proximal end of the supporting ridge opposite the first, distal end, such that the supporting ridge is disposed proximal to the first arched element and distal to the plurality of undulating transverse ridges, the plurality of undulating transverse ridges including at least two sets of undulating transverse ridges, each set of undulating transverse ridges extending around a circumference of the medical device;wherein the heart valve prosthesis remains fixedly attached to the medical device to function as a heart valve after removal of the catheter from the body, the heart valve prosthesis repeatedly opening and closing to allow and prevent blood flow, respectively, through the medical device.
  • 30. The medical device, in combination with a heart valve prosthesis of claim 29, further including an eyelet element connected to at least one of the plurality of undulating transverse ridges.
  • 31. The medical device, in combination with a heart valve prosthesis of claim 29, wherein the plurality of undulating transverse ridges form a supporting body configured to engage a portion of a vessel wall when the medical device is in the expanded mode at a deployed state.
  • 32. The medical device, in combination with a heart valve prosthesis of claim 29, wherein the device is configured to be implanted within an aorta.
  • 33. The medical device, in combination with a heart valve prosthesis of claim 29, wherein at least one of the plurality of undulating transverse ridges includes tips to facilitate anchoring of the device into tissue of a vessel or a heart of a patient.
  • 34. The medical device, in combination with a heart valve prosthesis of claim 29, wherein the plurality of undulating transverse ridges have a saw-tooth shape.
  • 35. The medical device, in combination with a heart valve prosthesis of claim 29, wherein the plurality of undulating transverse ridges have a rhombic shape.
  • 36. The medical device, in combination with a heart valve prosthesis of claim 29, wherein the heart valve prosthesis is a biological heart valve prosthesis.
  • 37. The medical device, in combination with a heart valve prosthesis of claim 29, wherein the heart valve prosthesis is an artificial heart valve prosthesis.
  • 38. The medical device, in combination with a heart valve prosthesis of claim 29, wherein the three sections are spaced substantially 120 degrees apart.
  • 39. The medical device, in combination with a heart valve prosthesis of claim 29, wherein the device is constructed from memory metal.
  • 40. The medical device, in combination with a heart valve prosthesis of claim 29, wherein the device is balloon expandable.
Priority Claims (1)
Number Date Country Kind
100 10 074 Feb 2000 DE national
PCT Information
Filing Document Filing Date Country Kind 371c Date
PCT/DE01/00837 2/28/2001 WO 00 11/25/2002
Publishing Document Publishing Date Country Kind
WO01/62189 8/30/2001 WO A
US Referenced Citations (277)
Number Name Date Kind
3755823 Hancock Sep 1973 A
4106129 Carpentier et al. Aug 1978 A
RE30912 Hancock Apr 1982 E
4922905 Strecker May 1990 A
4994077 Dobben Feb 1991 A
5002566 Carpentier et al. Mar 1991 A
5061277 Carpentier et al. Oct 1991 A
5094661 Levy et al. Mar 1992 A
5104407 Lam et al. Apr 1992 A
5163953 Vince Nov 1992 A
5197979 Quintero et al. Mar 1993 A
5234456 Silvestrini Aug 1993 A
5279612 Eberhardt Jan 1994 A
5332402 Teitelbaum Jul 1994 A
5336258 Quintero et al. Aug 1994 A
5342348 Kaplan Aug 1994 A
5352240 Ross Oct 1994 A
5368608 Levy et al. Nov 1994 A
5397351 Pavcnik et al. Mar 1995 A
5411552 Andersen et al. May 1995 A
5456713 Chuter Oct 1995 A
5476508 Amstrup Dec 1995 A
5509930 Love Apr 1996 A
5549666 Hata et al. Aug 1996 A
5595571 Jaffe et al. Jan 1997 A
5613982 Goldstein Mar 1997 A
5632778 Goldstein May 1997 A
5674298 Levy et al. Oct 1997 A
5679112 Levy et al. Oct 1997 A
5683451 Lenker et al. Nov 1997 A
5697972 Kim et al. Dec 1997 A
5713953 Vallana et al. Feb 1998 A
5746775 Levy et al. May 1998 A
5755777 Chuter May 1998 A
5824041 Lenker et al. Oct 1998 A
5824080 Lamuraglia Oct 1998 A
5840081 Andersen et al. Nov 1998 A
5841382 Walden et al. Nov 1998 A
5843181 Jaffe et al. Dec 1998 A
5853419 Imran Dec 1998 A
5855601 Bessler et al. Jan 1999 A
5876434 Flomenblit et al. Mar 1999 A
5880242 Hu et al. Mar 1999 A
5899936 Goldstein May 1999 A
5928281 Huynh et al. Jul 1999 A
5935163 Gabbay Aug 1999 A
5104407 Lam et al. Sep 1999 B1
5964798 Imran Oct 1999 A
6001126 Nguyen-Thien-Nhon Dec 1999 A
5061277 Carpentier et al. Feb 2000 B1
6077297 Robinson et al. Jun 2000 A
6093530 McIlroy et al. Jul 2000 A
6102944 Huynh et al. Aug 2000 A
6117169 Moe Sep 2000 A
6126685 Lenker et al. Oct 2000 A
6146417 Ischinger Nov 2000 A
6168614 Andersen et al. Jan 2001 B1
6177514 Pathak et al. Jan 2001 B1
6183481 Lee et al. Feb 2001 B1
6190405 Culombo et al. Feb 2001 B1
6200336 Pavcnik et al. Mar 2001 B1
6214055 Simionescu et al. Apr 2001 B1
6231602 Carpentier et al. May 2001 B1
6245102 Jayaraman Jun 2001 B1
6254564 Wilk et al. Jul 2001 B1
6254636 Peredo Jul 2001 B1
6283995 Moe et al. Sep 2001 B1
6287338 Sarnowski et al. Sep 2001 B1
6338740 Carpentier Jan 2002 B1
6342070 Nguyen-Thien-Nhon Jan 2002 B1
6344044 Fulkerson et al. Feb 2002 B1
6350278 Lenker et al. Feb 2002 B1
6379740 Rinaldi et al. Apr 2002 B1
6391538 Vyavahare et al. May 2002 B1
6425916 Garrison et al. Jul 2002 B1
6454799 Schreck Sep 2002 B1
6471723 Ashworth et al. Oct 2002 B1
6478819 Moe Nov 2002 B2
6508833 Pavcnik et al. Jan 2003 B2
6509145 Torrianni Jan 2003 B1
6521179 Girardot et al. Feb 2003 B1
6540782 Snyders Apr 2003 B1
6558417 Peredo May 2003 B2
6558418 Carpentier et al. May 2003 B2
6572642 Rinaldi et al. Jun 2003 B2
6582462 Andersen et al. Jun 2003 B1
6585766 Huynh et al. Jul 2003 B1
6613086 Moe et al. Sep 2003 B1
6626939 Burnside et al. Sep 2003 B1
6682559 Myers et al. Jan 2004 B2
6730118 Spenser et al. May 2004 B2
6736845 Marquez et al. May 2004 B2
6743252 Bates et al. Jun 2004 B1
6767362 Schreck Jul 2004 B2
6773455 Allen et al. Aug 2004 B2
6790230 Beyersdorf et al. Sep 2004 B2
6808529 Fulkerson Oct 2004 B2
6821211 Otten et al. Nov 2004 B2
6821297 Snyders Nov 2004 B2
6824970 Vyavahare et al. Nov 2004 B2
6830584 Seguin Dec 2004 B1
6861211 Levy et al. Mar 2005 B2
6872226 Cali et al. Mar 2005 B2
6881199 Wilk et al. Apr 2005 B2
6893460 Spenser et al. May 2005 B2
6908481 Cribier Jun 2005 B2
6911043 Myers et al. Jun 2005 B2
6945997 Huynh et al. Sep 2005 B2
6974474 Pavcnik et al. Dec 2005 B2
7014655 Barbarash et al. Mar 2006 B2
7018406 Seguin et al. Mar 2006 B2
7037333 Myers et al. May 2006 B2
7050276 Nishiyama May 2006 B2
7078163 Torrianni Jul 2006 B2
7081132 Cook et al. Jul 2006 B2
7137184 Schreck et al. Nov 2006 B2
7141064 Scott et al. Nov 2006 B2
7163556 Xie et al. Jan 2007 B2
7189259 Simionescu et al. Mar 2007 B2
7198646 Figulla et al. Apr 2007 B2
7201772 Schwammenthal et al. Apr 2007 B2
7238200 Lee et al. Jul 2007 B2
7252682 Seguin Aug 2007 B2
7267686 DiMatteo et al. Sep 2007 B2
7318278 Zhang et al. Jan 2008 B2
7318998 Goldstein et al. Jan 2008 B2
7322932 Xie et al. Jan 2008 B2
7329278 Seguin et al. Feb 2008 B2
7381218 Schreck Jun 2008 B2
7393360 Spenser et al. Jul 2008 B2
7399315 Iobbi Jul 2008 B2
7452371 Pavcnik et al. Nov 2008 B2
7473275 Marquez Jan 2009 B2
7704222 Wilk et al. Apr 2010 B2
7736327 Wilk et al. Jun 2010 B2
20010011187 Pavcnik et al. Aug 2001 A1
20010021872 Bailey et al. Sep 2001 A1
20010039450 Pavcnik et al. Nov 2001 A1
20020032481 Gabbay Mar 2002 A1
20020055775 Carpentier et al. May 2002 A1
20020111668 Smith Aug 2002 A1
20020123790 White et al. Sep 2002 A1
20020133226 Marquez et al. Sep 2002 A1
20020198594 Schreck Dec 2002 A1
20030027332 Lafrance et al. Feb 2003 A1
20030036791 Philipp et al. Feb 2003 A1
20030036795 Andersen et al. Feb 2003 A1
20030040792 Gabbay Feb 2003 A1
20030050694 Yang et al. Mar 2003 A1
20030055495 Pease et al. Mar 2003 A1
20030065386 Weadock Apr 2003 A1
20030114913 Spenser et al. Jun 2003 A1
20030125795 Pavcnik et al. Jul 2003 A1
20030130726 Thorpe et al. Jul 2003 A1
20030139796 Sequin et al. Jul 2003 A1
20030139803 Sequin et al. Jul 2003 A1
20030149476 Damm et al. Aug 2003 A1
20030153974 Spenser et al. Aug 2003 A1
20030195620 Huynh et al. Oct 2003 A1
20030236570 Cook et al. Dec 2003 A1
20040006380 Buck et al. Jan 2004 A1
20040039436 Spenser et al. Feb 2004 A1
20040049262 Obermiller et al. Mar 2004 A1
20040073289 Hartley et al. Apr 2004 A1
20040078950 Schreck et al. Apr 2004 A1
20040117004 Osborne et al. Jun 2004 A1
20040117009 Cali et al. Jun 2004 A1
20040148018 Carpentier et al. Jul 2004 A1
20040153145 Simionescu et al. Aug 2004 A1
20040186558 Pavcnik et al. Sep 2004 A1
20040186563 Lobbi Sep 2004 A1
20040186565 Schreck Sep 2004 A1
20040193244 Hartley et al. Sep 2004 A1
20040210301 Obermiller et al. Oct 2004 A1
20040210304 Seguin et al. Oct 2004 A1
20040260389 Case et al. Dec 2004 A1
20050009000 Wilhelm et al. Jan 2005 A1
20050033220 Wilk et al. Feb 2005 A1
20050033398 Seguin Feb 2005 A1
20050043790 Seguin Feb 2005 A1
20050049692 Numamoto et al. Mar 2005 A1
20050075725 Rowe Apr 2005 A1
20050075776 Cho Apr 2005 A1
20050096726 Sequin et al. May 2005 A1
20050096736 Osse et al. May 2005 A1
20050098547 Cali et al. May 2005 A1
20050113910 Paniagua et al. May 2005 A1
20050119728 Sarac Jun 2005 A1
20050119736 Zilla et al. Jun 2005 A1
20050137687 Salahieh et al. Jun 2005 A1
20050137688 Salahieh et al. Jun 2005 A1
20050137690 Salahieh et al. Jun 2005 A1
20050137697 Salahieh et al. Jun 2005 A1
20050137698 Salahieh et al. Jun 2005 A1
20050137702 Haug et al. Jun 2005 A1
20050143804 Haverkost Jun 2005 A1
20050143807 Pavcnik et al. Jun 2005 A1
20050149166 Schaeffer et al. Jul 2005 A1
20050150775 Zhang et al. Jul 2005 A1
20050171597 Boatman et al. Aug 2005 A1
20050171598 Schaeffer Aug 2005 A1
20050192665 Spenser et al. Sep 2005 A1
20050197695 Stacchino et al. Sep 2005 A1
20050222668 Schaeffer et al. Oct 2005 A1
20050234546 Nugent et al. Oct 2005 A1
20050267560 Bates Dec 2005 A1
20060009842 Huynh et al. Jan 2006 A1
20060025857 Bergheim et al. Feb 2006 A1
20060047343 Oviatt et al. Mar 2006 A1
20060058864 Schaeffer et al. Mar 2006 A1
20060074484 Huber Apr 2006 A1
20060111770 Pavcnik et al. May 2006 A1
20060142846 Pavcnik et al. Jun 2006 A1
20060149360 Schwammenthal et al. Jul 2006 A1
20060167543 Bailey et al. Jul 2006 A1
20060193885 Neethling et al. Aug 2006 A1
20060210597 Hiles Sep 2006 A1
20060229718 Marquez Oct 2006 A1
20060229719 Marquez et al. Oct 2006 A1
20060246584 Covelli Nov 2006 A1
20060259134 Schwammenthal et al. Nov 2006 A1
20060259136 Nguyen et al. Nov 2006 A1
20060265056 Nguyen et al. Nov 2006 A1
20060287717 Rowe et al. Dec 2006 A1
20060287719 Rowe et al. Dec 2006 A1
20060290027 O'Connor et al. Dec 2006 A1
20060293745 Carpentier et al. Dec 2006 A1
20070005129 Damm et al. Jan 2007 A1
20070005131 Taylor Jan 2007 A1
20070005132 Simionescu et al. Jan 2007 A1
20070020248 Everaerts et al. Jan 2007 A1
20070021826 Case et al. Jan 2007 A1
20070027535 Purdy, Jr. et al. Feb 2007 A1
20070038291 Case et al. Feb 2007 A1
20070038295 Case et al. Feb 2007 A1
20070043435 Seguin et al. Feb 2007 A1
20070050014 Johnson Mar 2007 A1
20070088431 Bourang et al. Apr 2007 A1
20070093887 Case et al. Apr 2007 A1
20070100435 Case et al. May 2007 A1
20070100440 Figulla et al. May 2007 A1
20070112422 Dehdashtian May 2007 A1
20070123700 Ueda et al. May 2007 A1
20070123979 Perier et al. May 2007 A1
20070142906 Figulla et al. Jun 2007 A1
20070162103 Case et al. Jul 2007 A1
20070173932 Cali et al. Jul 2007 A1
20070179592 Schaeffer Aug 2007 A1
20070185565 Schwammenthal et al. Aug 2007 A1
20070203576 Lee et al. Aug 2007 A1
20070213813 Von Segesser et al. Sep 2007 A1
20070239271 Nguyen Oct 2007 A1
20070244551 Stobie Oct 2007 A1
20070260327 Case et al. Nov 2007 A1
20070288087 Fearnot et al. Dec 2007 A1
20080004688 Spenser et al. Jan 2008 A1
20080021546 Patz et al. Jan 2008 A1
20080033534 Cook et al. Feb 2008 A1
20080065011 Marchand et al. Mar 2008 A1
20080071361 Tuval et al. Mar 2008 A1
20080071362 Tuval et al. Mar 2008 A1
20080071363 Tuval et al. Mar 2008 A1
20080071366 Tuval et al. Mar 2008 A1
20080071368 Tuval et al. Mar 2008 A1
20080071369 Tuval et al. Mar 2008 A1
20080077236 Letac et al. Mar 2008 A1
20080086205 Gordy et al. Apr 2008 A1
20080097586 Pavcnik et al. Apr 2008 A1
20080102439 Tian et al. May 2008 A1
20080133003 Seguin et al. Jun 2008 A1
20080140189 Nguyen et al. Jun 2008 A1
20080154355 Benichou et al. Jun 2008 A1
20080200977 Paul et al. Aug 2008 A1
20080215143 Seguin Sep 2008 A1
20080262602 Wilk et al. Oct 2008 A1
20080269878 Iobbi Oct 2008 A1
20080275549 Rowe Nov 2008 A1
Foreign Referenced Citations (177)
Number Date Country
19546692 Jun 1997 DE
19633901 Feb 1998 DE
20003874 Jun 2000 DE
19857887 Jul 2000 DE
10010073 Sep 2001 DE
10010074 Oct 2001 DE
101 21 210 Nov 2002 DE
19546692 Nov 2002 DE
10010074 Apr 2005 DE
19857887 May 2005 DE
10010073 Dec 2005 DE
0084395 Jul 1983 EP
0458877 Aug 1990 EP
0402036 Dec 1990 EP
0402176 Dec 1990 EP
0458877 Apr 1991 EP
0515324 Nov 1992 EP
0547135 Jun 1993 EP
0871414 Sep 1995 EP
0 592 410 Oct 1995 EP
0756498 Oct 1995 EP
0 592 410 Nov 1995 EP
0786970 May 1996 EP
0729364 Sep 1996 EP
0756498 May 1997 EP
0778775 Jun 1997 EP
0786970 Aug 1997 EP
0888142 Sep 1997 EP
0971649 Oct 1998 EP
0928615 Jul 1999 EP
1051204 Jul 1999 EP
1089676 Dec 1999 EP
0986348 Mar 2000 EP
1117446 Apr 2000 EP
1 164 976 Aug 2000 EP
1158937 Sep 2000 EP
1 251 805 Oct 2000 EP
1041942 Oct 2000 EP
1041943 Oct 2000 EP
1171061 Oct 2000 EP
1206179 Feb 2001 EP
1 233 731 May 2001 EP
1117446 Jul 2001 EP
1 255 510 Aug 2001 EP
1259193 Sep 2001 EP
1 233 731 May 2002 EP
1 330 213 May 2002 EP
1206179 May 2002 EP
1347785 Aug 2002 EP
1235537 Sep 2002 EP
1248655 Oct 2002 EP
1251804 Oct 2002 EP
1257305 Nov 2002 EP
0 971 649 Dec 2002 EP
1395208 Dec 2002 EP
1 401 359 Jan 2003 EP
1406561 Jan 2003 EP
1281357 Feb 2003 EP
1408882 Feb 2003 EP
1 435 878 Apr 2003 EP
1 435 879 Apr 2003 EP
1 441 672 Jun 2003 EP
1 017 868 Sep 2003 EP
1354569 Oct 2003 EP
1494616 Oct 2003 EP
1 519 697 Jan 2004 EP
1 539 047 Apr 2004 EP
1551274 Apr 2004 EP
1 560 542 May 2004 EP
1414295 May 2004 EP
1 603 493 Sep 2004 EP
1452153 Sep 2004 EP
0987998 Oct 2004 EP
1 087 727 Nov 2004 EP
1499366 Jan 2005 EP
1 663 070 Mar 2005 EP
1 253 875 Apr 2005 EP
1 667 614 Apr 2005 EP
1 251 803 Jun 2005 EP
1 702 247 Jul 2005 EP
1734902 Aug 2005 EP
1835948 Jun 2006 EP
1863545 Sep 2006 EP
1893132 Nov 2006 EP
1901681 Dec 2006 EP
1 255 510 Mar 2007 EP
1835948 Sep 2007 EP
1112042 Nov 2007 EP
1878407 Jan 2008 EP
1886649 Feb 2008 EP
1 900 343 Mar 2008 EP
1259195 Oct 2008 EP
1994913 Nov 2008 EP
2 000 115 Dec 2008 EP
2440809 Feb 2008 GB
52-086296 Jul 1977 JP
62-227352 Oct 1987 JP
2002-525169 Aug 2002 JP
2002-536115 Oct 2002 JP
2003-523262 Aug 2003 JP
2003-524504 Aug 2003 JP
2005-118585 May 2005 JP
2007-296375 Nov 2007 JP
WO-9009102 Aug 1990 WO
WO 9117720 Nov 1991 WO
WO-9524873 Sep 1995 WO
WO-9528183 Oct 1995 WO
WO-9613227 May 1996 WO
WO-9732615 Sep 1997 WO
WO-9843556 Oct 1998 WO
WO-9846165 Oct 1998 WO
WO-9937337 Jul 1999 WO
WO-9966863 Dec 1999 WO
WO 0015148 Mar 2000 WO
WO 0018333 Apr 2000 WO
WO-0018445 Apr 2000 WO
WO 0025702 May 2000 WO
WO 00047139 Aug 2000 WO
WO 0047139 Aug 2000 WO
WO-0053125 Sep 2000 WO
WO-0062714 Oct 2000 WO
WO-0110209 Feb 2001 WO
WO 0135870 May 2001 WO
WO-0141679 Jun 2001 WO
WO-0151104 Jul 2001 WO
WO 0154625 Aug 2001 WO
WO-0158503 Aug 2001 WO
WO 0162189 Aug 2001 WO
WO 0164137 Sep 2001 WO
WO 0236048 May 2002 WO
WO-02058745 Aug 2002 WO
WO-02100301 Dec 2002 WO
WO-02102286 Dec 2002 WO
WO 03003949 Jan 2003 WO
WO-03007795 Jan 2003 WO
WO-03009785 Feb 2003 WO
WO 03011195 Feb 2003 WO
WO 03013239 Feb 2003 WO
WO 03028592 Apr 2003 WO
WO 03047468 Jun 2003 WO
WO 00047139 Aug 2003 WO
WO-03079928 Oct 2003 WO
WO 03096935 Nov 2003 WO
WO 2004004597 Jan 2004 WO
WO 2004016200 Feb 2004 WO
WO 2004016201 Feb 2004 WO
WO 2004019825 Mar 2004 WO
WO-2004026117 Apr 2004 WO
WO 2004026173 Apr 2004 WO
WO 2004043301 May 2004 WO
WO 2004082527 Sep 2004 WO
WO 2004096100 Nov 2004 WO
WO 2005021063 Mar 2005 WO
WO 2005034812 Apr 2005 WO
WO 2005062980 Jul 2005 WO
WO 2005063980 Jul 2005 WO
WO-2005072654 Aug 2005 WO
WO 2006066327 Jun 2006 WO
WO-2006066327 Jun 2006 WO
WO 2006076890 Jul 2006 WO
WO-2006102063 Sep 2006 WO
WO 2006108090 Oct 2006 WO
WO 2006124649 Nov 2006 WO
WO-2006124649 Nov 2006 WO
WO 2006127756 Nov 2006 WO
WO 2006127765 Nov 2006 WO
WO-2006132948 Dec 2006 WO
WO 2007047488 Apr 2007 WO
WO 2007047945 Apr 2007 WO
WO 2007059252 May 2007 WO
WO-2007071436 Jun 2007 WO
WO 2007120543 Oct 2007 WO
WO-2008028569 Mar 2008 WO
WO 2008045949 Apr 2008 WO
WO 2008070797 Jun 2008 WO
WO 2008079962 Jul 2008 WO
WO 2008101083 Aug 2008 WO
Non-Patent Literature Citations (7)
Entry
Aortenklappenbioprothese erfolgreich in der Entwicklung, (1 page) May 16, 2003.
Translation of Aortenklappenbioprothese erfolgreich in der Entwicklung (2 pages).
Screen shots from http://www.fraunhofer.de/presse/filme/2006/index.jsp (2 pages), 2006.
Liang, Ma, et al., “Double-crowned valved stents for off-pump mitrel valve replacement,” European Journal of Cardio-Thoracic Surgery, 194-198 (5 pages), Jun. 13, 2005.
Huber, Christoph, et al. “Direct Access Valve Replacement (DAVR)—are we entering a new era in cardiac surgery?” European Journal of Cardio-Thoracic Surgery, 380-385, (6 pages), Jan. 19, 2006.
Translation of DE 19546692 A1 (4 pages).
File history for German Patent DE 195 46 692 filed Dec. 14, 1995 and patented Jul. 11, 2002.
Reissues (1)
Number Date Country
Parent 10204990 Feb 2001 US
Child 12213991 US