IP Library Granted Patent US 7,060,083
Granted Patent B2
US 7,060,083 · App. 10/152,441 · Granted Jun 13, 2006

Foldable vaso-occlusive member

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Quick Facts
Patent No.
US 7,060,083
App. No.
10/152,441
Granted
Jun 13, 2006
Kind
B2
Abstract

Vaso-occlusive devices for occlusion of a body cavity are provided. The vaso-occlusive devices include an elongate vaso-occlusive member having one or more fold lines. Methods of using the vaso-occlusive devices are also described.

Claims (68)

1. A vaso-occlusive device, comprising:

an elongate vaso-occlusive member, the vaso-occlusive member capable of assuming a desired folded configuration when the vaso-occlusive member is subjected to a force or pressure;

wherein the vaso-occlusive member defines and axis, and comprises a key-way that is disposed continuously along the axis of the vaso-occlusive member.

2. The vaso-occlusive device of claim 1 , wherein the key-way has a cross-sectional shape that is substantially rectangular.

3. The vaso-occlusive device of claim 1 , wherein the key-way has a cross-sectional shape tat is substantially triangular.

4. The vaso-occlusive device of claim 1 , wherein a width of the key-way varies.

5. The vaso-occlusive device of claim 1 , wherein a depth of the key-way varies.

6. The vaso-occlusive device of claim 1 , wherein the key-way exhibits a pitch.

7. The vaso-occlusive device of claim 6 , wherein the pitch of the key-way varies.

8. The vaso-occlusive device of claim 6 , wherein the pitch of the key-way is constant.

9. The vaso-occlusive device of claim 1 , wherein the key-way is disposed along a portion of the vaso-occlusive member in a helical fashion.

10. The vaso-occlusive device of claim 1 , wherein pitch of the key-way is relatively tight along a portion of the vaso-occlusive member.

11. The vaso-occlusive device of claim 1 , further comprising another key-way disposed continuously along a portion of the vaso-occlusive member.

12. The vaso-occlusive device of claim 11 , wherein the key-way and the other key-way are axially spaced from each other.

13. The vaso-occlusive device of claim 11 , wherein the key-way and the other key-way intersect.

14. The vaso-occlusive device of claim 1 , wherein the key-way is disposed discretely along the vaso-occlusive member.

15. The vaso-occlusive device of claim 14 , wherein the key-way is partially disposed about a portion of the circumference of the vaso-occlusive member.

16. The vaso-occlusive device of claim 14 , wherein the key-way is completely disposed about the circumference of the vaso-occlusive member.

17. The vaso-occlusive device of claim 14 , further comprising another key-way disposed discretely along the vaso-occlusive member.

18. The vaso-occlusive device of claim 17 , wherein the key-way and the another key-way are closely spaced.

19. The vaso-occlusive device of claim 1 , wherein the vaso-occlusive member is made of a biodegradable material.

20. The vaso-occlusive device of claim 1 , wherein the vaso-occlusive member comprises a metal selected from the group consisting of platinum, palladium, rhodium, gold, tungsten, and their alloys.

21. The vaso-occlusive device of claim 20 , wherein the vaso-occlusive member comprises an alloy of platinum and tungsten.

22. The vaso-occlusive device of claim 1 , wherein the vaso-occlusive member comprises an alloy selected from stainless steels and super-elastic alloys.

23. The vaso-occlusive device of claim 22 , wherein the vaso-occlusive member comprises nitinol.

24. The vaso-occlusive device of claim 1 , wherein the vaso-occlusive member is substantially rectilinear when in a relaxed configuration.

25. The vaso-occlusive device of claim 1 , wherein the vaso-occlusive member is substantially curvilinear when in a relaxed configuration.

26. The vaso-occlusive device of claim 1 , wherein the vaso-occlusive member has a secondary relaxed configuration.

27. The vaso-occlusive device of claim 26 , wherein the vaso-occlusive member is a helically wounded coil in the secondary relaxed configuration.

28. The vaso-occlusive device of claim 26 , wherein the vaso-occlusive member has a tertiary relaxed configuration.

29. The vaso-occlusive device of claim 1 , wherein the vaso-occlusive member is coupled to a deployment mechanism.

30. The vaso-occlusive device of claim 29 , wherein the deployment mechanism comprises an electrolytically severable junction adapted to detach from a core wire by imposition of an electric current on the core wire.

31. The vaso-occlusive device of claim 1 , wherein the vaso-occlusive member is sized to fit within an aneurysm.

32. The vaso-occlusive device of claim 1 , wherein a discrete portion of the vaso-occlusive member is made of a relatively flexible material for allowing the vaso-occlusive member to bend at the discrete portion.

33. A catheter assembly for occluding a body cavity, comprising:

a delivery catheter having a distal end; and

a vaso-occlusive device detachably coupled to the distal end of the catheter, the vaso-occlusive device defines and axis, and comprising an elongate vaso-occlusive member, the vaso-occlusive member having a fold line, wherein the vaso-occlusive member comprises a key-way for forming the fold line, and the key-way is disposed continuously along the axis of the vaso-occlusive member.

34. The catheter assembly of claim 33 , wherein the key-way has a cross-sectional shape that is substantially rectangular.

35. The catheter assembly of claim 33 , wherein the key-way has a cross-sectional shape that is substantially triangular.

36. The catheter assembly of claim 33 , wherein a width of the key-way varies.

37. The catheter assembly of claim 33 wherein a depth of the key-way varies.

38. The catheter assembly of claim 33 wherein the key-way exhibits a pitch.

39. The catheter assembly of claim 38 , wherein the pitch of the key-way varies.

40. The catheter assembly of claim 38 , wherein the pitch of the key-way is constant.

41. The catheter assembly of claim 33 , wherein the key-way is disposed along a portion of the vaso-occlusive member in a helical fashion.

42. The catheter assembly of claim 33 , wherein pitch of the key-way is relatively tight along a portion of the vaso-occlusive member.

43. The catheter assembly of claim 33 , wherein the vaso-occlusive device further comprises another key-way disposed continuously along a portion of the vaso-occlusive member.

44. The catheter assembly of claim 43 , wherein the key-way and the other key-way are axially spaced from each other.

45. The catheter assembly of claim 43 , wherein the key-way and the other key-way intersect.

46. The catheter assembly of claim 33 , wherein the key-way is disposed discretely along the vaso-occlusive member.

47. The catheter assembly of claim 46 , wherein the key-way is partially disposed about a portion of the circumference of the vaso-occlusive member.

48. The catheter assembly of claim 46 , wherein the key-way is completely disposed about the circumference of the vaso-occlusive member.

49. The catheter assembly of claim 46 , wherein the vaso-occlusive device further comprises another key-way disposed discretely along the vaso-occlusive member.

50. The catheter assembly of claim 49 , wherein the key-way and the another key-way are closely spaced.

51. The catheter assembly of claim 49 , wherein the vaso-occlusive member is made of a biodegradable material.

52. The catheter assembly of claim 33 , wherein the vaso-occlusive member comprises a metal selected from the group consisting of platinum, palladium, rhodium, gold, tungsten, and their alloys.

53. The catheter assembly of claim 52 , wherein the vaso-occlusive member comprises an alloy of platinum and tungsten.

54. The catheter assembly of claim 33 , wherein the vaso-occlusive member comprises an alloy selected from stainless steels and super-elastic alloys.

55. The catheter assembly of claim 54 , wherein the vaso-occlusive member comprises nitinol.

56. The catheter assembly of claim 33 , wherein the vaso-occlusive member is substantially rectilinear when in a relaxed configuration.

57. The catheter assembly of claim 33 , wherein the vaso-occlusive member is substantially curvilinear when in a relaxed configuration.

58. The catheter assembly of claim 33 , wherein the vaso-occlusive member has a secondary relaxed configuration.

59. The catheter assembly of claim 58 , wherein the vaso-occlusive member is a helically wounded coil in the secondary relaxed configuration.

60. The catheter assembly of claim 58 , wherein the vaso-occlusive member has a tertiary relaxed configuration.

61. The catheter assembly of claim 33 , further comprising a deployment mechanism coupled to a proximal end of the vaso-occlusive member.

62. The catheter assembly of claim 61 , wherein the deployment mechanism comprises an electrolytically severable junction adapted to detach from a core wire by imposition of an electric current on the core wire.

63. The catheter assembly of claim 33 , wherein the vaso-occlusive member is sized to fit within an aneurysm.

64. The catheter assembly of claim 33 , wherein a portion of the vaso-occlusive member is made of a relatively weaker material for forming the fold line.

Assignments (8)
NUNC PRO TUNC ASSIGNMENT Recorded Jun 7, 2020
From: STRYKER EUROPEAN HOLDINGS I, LLC
To: STRYKER EUROPEAN HOLDINGS III, LLC
Reel/Frame 052861/0001 →
CHANGE OF NAME Recorded Jun 7, 2020
From: STRYKER EUROPEAN HOLDINGS III, LLC
To: STRYKER EUROPEAN OPERATIONS HOLDINGS LLC
Reel/Frame 052860/0716 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT SERIAL # 09/905,670 AND 07/092,079 PREVIOUSLY RECORDED AT REEL: 037153 FRAME: 0034. ASSIGNOR(S) HEREBY CONFIRMS THE NUNC PRO TUNC ASSIGNMENT. Recorded Mar 8, 2016
From: STRYKER NV OPERATIONS LIMITED
To: STRYKER MEDTECH LIMITED
Reel/Frame 038039/0001 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT LISTED SERIAL NOS. 09/905,670 AND 07/092,079 PREVIOUSLY RECORDED AT REEL: 037153 FRAME: 0241. ASSIGNOR(S) HEREBY CONFIRMS THE NUNC PRO TUNC ASSIGNMENT EFFECTIVE DATE 9/29/2014. Recorded Mar 8, 2016
From: STRYKER MEDTECH LIMITED
To: STRYKER EUROPEAN HOLDINGS I, LLC
Reel/Frame 038043/0011 →
NUNC PRO TUNC ASSIGNMENT Recorded Nov 23, 2015
From: STRYKER NV OPERATIONS LIMITED
To: STRYKER MEDTECH LIMITED
Reel/Frame 037153/0034 →
NUNC PRO TUNC ASSIGNMENT Recorded Nov 23, 2015
From: STRYKER MEDTECH LIMITED
To: STRYKER EUROPEAN HOLDINGS I, LLC
Reel/Frame 037153/0241 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2011
From: BOSTON SCIENTIFIC SCIMED, INC.
To: STRYKER CORPORATION; STRYKER NV OPERATIONS LIMITED
Reel/Frame 025969/0841 →
CHANGE OF NAME Recorded Nov 6, 2006
From: SCIMED LIFE SYSTEMS, INC.
To: BOSTON SCIENTIFIC SCIMED, INC.
Reel/Frame 018505/0868 →