Inflatable multi-chambered devices and methods of treatment using the same

Patent metadata

Field	Value
Publication number	US-9408709-B2
Application number	US-201313891677-A
Country	US
Kind code	B2
Filing date	May 10, 2013
Priority date	Jun 12, 2006
Publication date	Aug 9, 2016
Grant date	Aug 9, 2016

Abstract

Inflatable multi-chambered devices are provided for repairing or replacing spinal discs and distracting neighboring vertebral elements. Also included are cushioning devices that may be used in a joint replacement device cushioning system. Further included are kits and systems that include such devices, methods for making such devices, and methods of treating patients in need of such devices. Examples further include cosmetic augmentation and restoration devices.

First claim

What is claimed is:

1. A surgical method comprising:
providing an implant, wherein the implant includes a deflated configuration and an inflated configuration whereby at least a portion of the implant is expanded to a size greater than in the deflated configuration;
inserting the implant into a disc space of a patient in the deflated configuration; and
inflating the implant within the disc space of the patient,
wherein the implant comprises at least three chambers arranged side-by-side and a filling manifold for providing access to at least one of the chambers in order to provide a filling material therein, and wherein the at least three chambers comprise adjacent concentric hollow cylindrical tube chambers.

2. The method of claim 1 , wherein the at least three chambers are independent chambers in which filling material does not pass therebetween.

3. The method of claim 1 , wherein the at least three chambers are interrelated chambers in which filling material does pass therebetween.

4. The method of claim 1 , wherein the filling manifold comprises a rotating ball valve.

5. The method of claim 1 , wherein the at least three chambers are formed of a flexible polymer.

6. The method of claim 1 , wherein the filling material comprises a non-resorbable hydrogel.

7. A surgical method comprising:
providing an implant, wherein the implant includes a deflated configuration and an inflated configuration whereby at least a portion of the implant is expanded to a size greater than in the deflated configuration;
inserting the implant through a cannula into a patient in the deflated configuration; and
inflating the implant within the patient,
wherein the implant comprises at least three chambers and a filling manifold for providing access to at least one of the chambers in order to provide a filling material therein, and wherein the at least three chambers comprise adjacent concentric hollow cylindrical tube chambers.

8. The method of claim 7 , further comprising filling each of the at least three chambers individually with a filling material.

9. The method of claim 7 , wherein the filling manifold comprises at least one rotating ball valve adapted to allow a filler medium to be inserted at least partially concurrently into at least two of the chambers.

10. The method of claim 7 , wherein the filler medium is at least one material selected from the group consisting of hydrogel, air, water, and saline.

11. The method of claim 7 , wherein the implant further comprises a pressure detector within at least one of said chambers.

12. A surgical method comprising:
providing an implant, wherein the implant includes a deflated configuration and an inflated configuration whereby at least a portion of the implant is expanded to a size greater than in the deflated configuration;
inserting the implant into a patient in the deflated configuration; and
inflating the implant within the patient,
wherein the implant comprises at least three independent, adjacent, hollow tube chambers comprising a flexible polymer material, wherein each tube is curved to form a ring and the rings are arranged concentrically around an axis, and wherein the implant further comprises at least one filling manifold adapted to allow a filler material to be inserted into at least one of the chambers.

13. The method of claim 12 , wherein the filler material is at least one material selected from the group consisting of hydrogel, air, water, and saline.

14. The method of claim 12 , wherein the implant comprises a pressure detector within at least one of said chambers.

15. The method of claim 12 , wherein the implant comprises a sealing means to prevent filler material from entering or exiting at least one of the chambers.

16. The method of claim 12 , wherein the at least three chambers are surrounded by a reinforcing material.

17. The method of claim 12 , wherein the implant is implanted for at least one of the following: replacement or augmentation of nucleus pulposus; distraction of neighboring vertebral elements; cushioning in a joint replacement system; plastic surgery augmentation, reconstruction, restoration, or tissue expansion; and damping, positioning, or isolation in a mechanical system.

18. The method of claim 12 , wherein the at least one filling manifold comprises a rotating valve.

Assignees

• Globus Medical Inc

Inventors

• Wirtel Iii Anthony
• Borden Mark

Classifications

• A61F2/4241

  for hands, e.g. fingers · CPC title

• A61F2250/0098

  radio-opaque, e.g. radio-opaque markers · CPC title

• A61F2002/30062

  (bio)absorbable, biodegradable, bioerodable, (bio)resorbable, resorptive · CPC title

• A61F2230/0065

  toroidal, e.g. ring-shaped, doughnut-shaped · CPC title

• A61F2250/0063

  Nested prosthetic parts · CPC title