IP Library › Granted Patent US 8,380,311
Granted Patent B2
US 8,380,311 · App. 11/590,250 · Granted Feb 19, 2013

Housing for implantable medical device

Inventors: Bernard Q. Li (Plymouth, MN); John J. Grevious (Minneapolis, MN); Timothy J. Davis (Coon Rapids, MN); Leroy Perz (Buffalo, MN); Chris J. Paidosh (St. Anthony, MN)
Assignee: Medtronic, Inc.
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Quick Facts
Patent No.
US 8,380,311
App. No.
11/590,250
Granted
Feb 19, 2013
Kind
B2
Abstract

A housing for an implantable medical device includes a first portion formed from a first material and a second portion formed from a second material. The first material and the second material comprise titanium and the first material has a higher resistivity than the second material.

Claims (56)

1. A housing for an implantable medical device comprising:

a first portion formed from a first material and aligned with a coil provided within the housing; and

a second portion formed from a second material that differs from the first material;

wherein the first material and the second material each comprise titanium and the first material has a higher resistivity than the second material; and

wherein the second portion includes an aperture extending entirely through a generally planar region of a wall thereof at a first location, and the first portion is coupled to the second portion at the first location to seal the aperture, such that the first portion forms a part of the wall.

2. The housing of claim 1 , wherein the first portion has a generally planar configuration.

3. The housing of claim 1 , wherein the first portion is welded to the second portion.

4. The housing of claim 1 , wherein the second material comprises commercial pure Grade 1 titanium.

5. The housing of claim 4 , wherein the first material comprises an alloy having the formula Ti-4.5Al-3V-2Fe-2Mo-0.15O.

6. The housing of claim 4 , wherein the first material comprises an alloy having the formula Ti-4Al-2.5V-1.5Fe-0.25O.

7. The housing of claim 4 , wherein the first material comprises an alloy having the formula Ti-6Al-2Sn-4Zr-2Mo.

8. The housing of claim 4 , wherein the first material comprises an alloy having the formula Ti-3Al-2.5V.

9. The housing of claim 4 , wherein the first material comprises an alloy having the formula Ti-6Al-4V.

10. The housing of claim 4 , wherein the first material comprises an alloy having the formula Ti-8Al-1Mo-1V.

11. The housing of claim 4 , wherein the first material comprises a titanium matrix composite.

12. The housing of claim 1 , wherein the first material is an alloy selected from the group consisting of Ti-4.5Al-3V-2Fe-2Mo-0.15O, Ti-4Al-2.5V-1.5Fe-0.25O, Ti-6Al-2Sn-4Zr-2Mo, Ti-3Al-2.5V, Ti-6Al-4V, Ti-8Al-1Mo-1V and combinations thereof.

13. The housing of claim 12 , wherein the second material is an alloy selected from the group consisting of Ti-4.5Al-3V-2Fe-2Mo-0.15O, Ti-4Al-2.5V-1.5Fe-0.25O, Ti-6Al-2Sn-4Zr-2Mo, Ti-3Al-2.5V, Ti-6Al-4V, Ti-8Al-1Mo-1V and combinations thereof.

14. The housing of claim 1 , wherein the second material is an alloy selected from the group consisting of Ti-4.5Al-3V-2Fe-2Mo-0.15O, Ti-4Al-2.5V-1.5Fe-0.25O, Ti-6Al-2Sn-4Zr-2Mo, Ti-3Al-2.5V, Ti-6Al-4V, Ti-8Al-1Mo-1V and combinations thereof.

15. The housing of claim 1 , wherein the second portion has a wall thickness of between approximately 0.001 and 0.016 inches.

16. The housing of claim 1 , wherein at least a portion of the housing has a radius of curvature of between approximately 0.1 and 2.5 millimeters.

17. The housing of claim 1 , wherein the second material exhibits greater formability as compared to a Ti-6Al-4V alloy.

18. The housing of claim 1 , wherein the second material has better formability than the first material.

19. The housing of claim 1 , wherein the housing is configured for use as the housing for an implantable neurological stimulation device.

20. The housing of claim 1 , wherein the housing exhibits improved telemetry performance as compared to a housing made entirely of commercial pure titanium Grade 1.

21. The housing of claim 1 , wherein the first portion has a higher resistivity than the second portion.

22. The housing of claim 1 , wherein the wherein the second portion is not formed from the first material.

23. The housing of claim 22 , wherein the first portion is not formed from the second material.

24. An implantable neurological stimulation device comprising:

a housing comprising a first portion and a second portion, the first portion and the second portion defining different regions of an innermost surface of the housing; and

a coil provided within the housing;

wherein the first portion comprises a first titanium material and the second portion comprises a second titanium material different from the first titanium material, the first portion being provided proximate the coil and having a higher resistivity than the second portion.

25. The implantable neurological stimulation device of claim 24 , wherein the first portion has a generally planar configuration.

26. The implantable neurological stimulation device of claim 24 , wherein the first portion is welded to the second portion.

27. The implantable neurological stimulation device of claim 24 , wherein the first titanium material is an alloy selected from the group consisting of Ti-4.5Al-3V-2Fe-2Mo-0.15O, Ti-4Al-2.5V-1.5Fe-0.25O, Ti-6Al-2Sn-4Zr-2Mo, Ti-3Al-2.5V, Ti-6Al-4V, Ti-8Al-1Mo-1V and combinations thereof.

28. The implantable neurological stimulation device of claim 27 , wherein the second titanium material is an alloy selected from the group consisting of Ti-4.5Al-3V-2Fe-2Mo-0.15O, Ti-4Al-2.5V-1.5Fe-0.25O, Ti-6Al-2Sn-4Zr-2Mo, Ti-3Al-2.5V, Ti-6Al-4V, Ti-8Al-1Mo-1V and combinations thereof.

29. The implantable neurological stimulation device of claim 27 , wherein the second titanium material is commercial pure titanium Grade 1.

30. The implantable neurological stimulation device of claim 27 , wherein the second titanium material is an alloy selected from the group consisting of Ti-4.5Al-3V-2Fe-2Mo-0.15O, Ti-4Al-2.5V-1.5Fe-0.25O, Ti-6Al-2Sn-4Zr-2Mo, Ti-3Al-2.5V, Ti-6Al-4V, Ti-8Al-1Mo-1V and combinations thereof.

31. The implantable neurological stimulation device of claim 24 , wherein the second portion has a wall thickness of between approximately 0.001 and 0.016 inches.

32. The implantable neurological stimulation device of claim 24 , wherein at least a portion of the housing has a radius of curvature of between approximately 0.1 and 2.5 millimeters.

33. The implantable neurological stimulation device of claim 24 , wherein the second titanium material has better formability than the first titanium material.

34. The implantable neurological stimulation device of claim 24 , wherein the coil is a recharging coil.

35. The implantable neurological stimulation device of claim 24 , wherein the coil is a telemetry coil.

36. A method of producing an implantable medical device comprising:

coupling a first member to a second member to form a housing, the first member comprising a first titanium material and the second member comprising a second titanium material that is different from the first titanium material, the first titanium material having a higher resistivity than the second titanium material;

removing a portion of the second member to form an aperture therein; and

providing a coil within the housing;

wherein the first member is provided proximate the coil, the aperture extends completely through a wall of the second member, and the first member is coupled to the second member at the aperture, such that the first member forms a part of the wall.

37. The method of claim 36 , wherein the first member is coupled to the second member to seal the aperture.

38. The method of claim 36 , wherein the step of coupling the first member to the second member comprises welding the first member to the second member.

39. The method of claim 36 , wherein the first titanium material comprises Grade 1 titanium and the second titanium material is selected from the group consisting of Ti-4.5Al-3V-2Fe-2Mo-0.15O, Ti-4Al-2.5V-1.5Fe-0.25O, Ti-6Al-2Sn-4Zr-2Mo, Ti-3Al-2.5V, Ti-6Al-4V, Ti-8Al-1Mo-1V and combinations thereof.

40. The method of claim 36 , wherein the first titanium material and the second titanium material are each selected from the group consisting of Ti-4.5Al-3V-2Fe-2Mo-0.15O, Ti-4Al-2.5V-1.5Fe-0.25O, Ti-6Al-2Sn-4Zr-2Mo, Ti-3Al-2.5V, Ti-6Al-4V, Ti-8Al-1Mo-1V and combinations thereof.

41. The method of claim 36 , wherein the second titanium material is selected from the group consisting of Ti-4.5Al-3V-2Fe-2Mo-0.15O, Ti-4Al-2.5V-1.5Fe-0.25O, Ti-6Al-2Sn-4Zr-2Mo, Ti-3Al-2.5V, Ti-6Al-4V, Ti-8Al-1Mo-1V and combinations thereof.

42. The method of claim 36 , wherein the second titanium material has better formability than the first titanium material.

43. The method of claim 36 , wherein the second titanium material has greater percent elongation at room temperature as compared to the first titanium material.

44. The method of claim 36 , wherein the coil is a telemetry coil.

45. The method of claim 36 , wherein the coil is a recharging coil.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2007
From: LI, BERNARD Q.; GREVIOUS, JOHN J.; DAVIS, TIMOTHY J.; PERZ, LEROY; PAIDOSH, CHRIS J.
To: MEDTRONIC, INC.
Reel/Frame 018754/0870 →
Continuity (1)
Related Publication 20080103556A1 · May 1, 2008