Dynamized interspinal implant

• US 9,662,147 B2
• Filed: 05/06/2016
• Issued: 05/30/2017
• Est. Priority Date: 03/06/2004
• Status: Active Grant

• Current Assignee: Depuy Synthes Products Incorporated (Johnson & Johnson)
• Original Assignee: Depuy Synthes Products Incorporated (Johnson & Johnson)
• Inventors: DiNello, Alexander Michel, Serhan, Hassan, Christianson, William
• Primary Examiner(s): Philogene, Pedro
• Assistant Examiner(s): Comstock, David C
• Application Number:
  US15/148,937
• Publication Number:
  US 20160249958A1
• Time in Patent Office: 389 Days
• Field of Search: 606246-249, 606279, 623 1711, 623 1713, 623 1715, 623 1716
• CPC Class Codes: A61B 17/7062 Devices acting on, attached to, or simulating the effect of, vertebral processes, vertebral facets or ribs rib fixation devices A61B17/8076; Tools for such devices
• CPC Class Codes: A61B 17/7065 Devices with changeable shape, e.g. collapsible or having retractable arms to aid implantation; Tools therefor
• CPC Class Codes: A61B 17/7068 Devices comprising separate rigid parts, assembled in situ, to bear on each side of spinous processes; Tools therefor
• CPC Class Codes: A61B 2017/00075 Motion
• CPC Class Codes: A61B 2017/00221 with wireless transmission of data, e.g. by infrared radiation or radiowaves
• CPC Class Codes: A61B 2017/00964 composite
• CPC Class Codes: A61B 2017/567 Joint mechanisms or joint supports in addition to the natural joints and outside the joint gaps
• CPC Class Codes: A61B 2017/681 Alignment, compression, or distraction mechanisms
• CPC Class Codes: A61F 2/4405 for apophyseal or facet joints, i.e. between adjacent spinous or transverse processes devices implanted between spinous or transverse processes A61B17/7062
• CPC Class Codes: A61F 2/482 Electrical means

Abstract

An interspinous process having a narrowed distal portion.

Claims

1. A method of treating a patient having a spinal pathology within a functional spinal unit (FSU) having an upper vertebra, a lower vertebra, and an intervertebral disc therebetween, the method comprising:

damaging an anterior longitudinal ligament (ALL) of the patient, thereby increasing the range of motion of the FSU in extension,

inserting an interbody device into a void between the upper and lower vertebrae, the interbody device comprising;

a) an upper portion having an upper surface adapted for bearing against the upper vertebra and having teeth extending therefrom for gripping the upper vertebra,

b) a lower portion having a lower surface adapted for bearing against the lower vertebra and having teeth extending therefrom for gripping the lower vertebra, and

c) a wall connecting the upper and lower portions,

wherein the upper and lower portions of the device are non-parallel.

2. The method of claim 1, wherein the upper and lower surfaces of the device are non-parallel.

3. The method of claim 2, wherein the non-parallel upper and lower surfaces of the device form an angle of at least 20 degrees.

4. The method of claim 1, wherein the device is disposed in the void in an orientation such that the distance between the upper and lower portions narrows as those portions extend toward the posterior longitudinal ligament (PLL).

5. The method of claim 1, wherein insertion of the device results in a restriction of the motion of the FSU.

6. The method of claim 1, wherein insertion of the device results in restriction of the motion of the FSU to less than 5 degrees in extension.

7. The method of claim 1, wherein the device further comprises:

d) an upper extension extending above the upper surface and having at least one transverse hole having a bone fastener received therein.

8. The method of claim 1, wherein the device further comprises:

d) a lower extension extending beneath the lower surface and having at least one transverse hole having a bone fastener received therein.

9. The method of claim 1, wherein the device further comprises at least one transverse hole having a bone fastener received therein.

10. The method of claim 9, wherein the bone fastener has a longitudinal axis extending substantially in the coronal plane.

11. The method of claim 1, further comprising a cavity between the upper and lower portions of the device.

12. The method of claim 1, wherein a length of the device is at least twice a width of the device.

13. The method of claim 1, wherein a length of the device is at least three times a width of the device.

14. The method of claim 1, wherein a first dimension of the device selected from length and width in a plane transverse to the spinal axis is at least twice as great as a second dimension of the device selected from length and width in the plane transverse to the spinal axis.

15. A method of treating a patient having a spinal pathology within a functional spinal unit (FSU) having an upper vertebra, a lower vertebra, and an intervertebral disc therebetween, the method comprising:

damaging an anterior longitudinal ligament (ALL) of the patient, thereby increasing the range of motion of the FSU in extension,

inserting an interbody device into a void between the upper and lower vertebrae, the interbody device comprising;

a) an upper portion having an upper surface adapted for bearing against the upper vertebra and having teeth extending therefrom for gripping the upper vertebra,

b) a lower portion having a lower surface adapted for bearing against the lower vertebra and having teeth extending therefrom for gripping the lower vertebra,

c) a wall connecting the upper and lower portions,

d) an upper extension extending above the upper surface and having at least one transverse hole having an upper bone fastener received therein, wherein the upper bone fastener has a longitudinal axis extending substantially in a coronal plane of the patient, and

e) a lower extension extending beneath the lower surface and having at least one transverse hole having a lower bone fastener received therein, wherein the lower bone fastener has a longitudinal axis extending substantially in the coronal plane of the patient,

wherein the upper and lower portions of the device are non-parallel,

wherein a first dimension of the device selected from length and width in a transverse plane of the patient is at least twice as great as a second dimension of the device selected from length and width in the transverse plane of the patient.

16. The method of claim 15, wherein the upper and lower surfaces of the device form an angle of at least 20 degrees.

17. The method of claim 15, wherein the first dimension is at least 3 times as great as the second dimension.

18. The method of claim 15, wherein a posterior edge of the upper extension and a posterior edge of the lower extension lie substantially in a common plane.

19. An intervertebral device, comprising:

a) an upper portion having an upper surface adapted for bearing against an upper vertebra and having teeth extending therefrom for gripping the upper vertebra,

b) a lower portion having a lower surface adapted for bearing against a lower vertebra and having teeth extending therefrom for gripping the lower vertebra, wherein the upper and lower portions of the device extend in a non-parallel manner in a first direction,

c) a wall connecting the upper and lower portions,

d) an upper extension extending above the upper surface and having at least one transverse hole having an upper bone fastener received therein, wherein the upper bone fastener has a longitudinal axis extending substantially transversely from the first direction, and

e) a lower extension extending beneath the lower surface and having at least one transverse hole having a lower bone fastener received therein, wherein the lower bone fastener has a longitudinal axis extending substantially transversely from the first direction.

20. The device of claim 19, wherein the device has a height that narrows in the first direction.

21. The device of claim 19, wherein a length of the device is at least twice a width of the device.

22. The device of claim 19, wherein a first dimension of the device selected from length and width in a plane transverse to the spinal axis is at least twice as great as a second dimension of the device selected from length and width in the plane transverse to the spinal axis.

23. The device of claim 19, wherein the length of the upper extension is less than the length of the upper portion.

24. The device of claim 19, wherein the thickness of the wall is greater than the thickness of the upper portion.

25. The device of claim 19, wherein a posterior edge of the upper extension and a posterior edge of the lower extension lie substantially in a common plane.

26. An intervertebral device, comprising:

a) an upper portion having an upper surface adapted for bearing against an upper vertebra and having teeth extending therefrom for gripping the upper vertebra,

b) a lower portion having a lower surface adapted for bearing against a lower vertebra and having teeth extending therefrom for gripping the lower vertebra,

c) a wall connecting the upper and lower portions,

d) an upper extension extending above the upper surface and having at least one transverse hole having an upper bone fastener received therein, and

e) a lower extension extending beneath the lower surface and having at least one transverse hole having a lower bone fastener received therein,

the device defining a height between a posterior end of the upper surface of the upper portion and a posterior end of the lower surface of the lower portion, wherein the height is adjustable under an axial load.

27. The device of claim 26, wherein the upper and lower portions of the device extend in a non-parallel manner in a first direction.

28. The device of claim 27, wherein the lower bone fastener has a longitudinal axis extending substantially transversely from the first direction.

29. The device of claim 26, wherein a posterior edge of the upper extension and a posterior edge of the lower extension lie substantially in a common plane.