Implant for reinforcing and annulus fibrosis
Reinforcement of annulus fibrosis tissue within an intervertebral disc can be achieved through implantation of a support member also functioning as a barrier to resist damage to the tissue or herniation of tissue outside of the disc. The device may be anchored to the surrounding tissue. The device is compressible and may be delivered in a minimally invasive manner through a cannula.
1. An implant for reinforcing an annulus of an intervertebral disc, comprising:
a barrier having a first surface for placement against an interior surface of an annulus lamella and a second opposing surface, wherein said barrier is adapted to be sealably positioned against the lamella via the exertion of force on at least a portion of the second surface sustained by a pressurized intervertebral disc environment;
wherein the barrier has a length corresponding to at least the length of the posterior annulus and a height corresponding to at least the distance between opposing vertebral endplates adjacent the intervertebral disc,
wherein a natural flow or egress of material from the nucleus to the anulus occurs along a longitudinal axis, wherein said longitudinal access is parallel to the height of said barrier;
wherein said material comprises endogenous nucleus pulposus or prosthetic augmentation material;
wherein said barrier has a thickness in a range of about 0.025 mm to about 2.5 mm;
wherein said barrier provides a seal and comprises a rigidity that prevents natural flow or egress of material beyond said barrier along said longitudinal axis,
wherein said barrier closes or barricades the area to be sealed to recreate the closed isobaric environment of a healthy disc nucleus;
wherein said length is greater than said height;
wherein the implant has a pre-formed concavity and is thereby inherently concave along at least a portion of said length; and
wherein the barrier comprises an enlarger,
wherein the enlarger expands the barrier and
wherein the enlarger contacts a substantial portion of the barrier and supports the barrier at its midpoint.
2. The implant of claim 1 , wherein the implant is concave along at least a portion of said first surface and convex along at least a portion of said second surface.
3. The implant of claim 1 , wherein said length and said height are dimensioned to prevent the barrier from slipping after insertion in the intervertebral disc.
4. The implant of claim 1 , wherein said length and said height are dimensioned to distribute pressure along the annulus.
5. The implant of claim 1 , wherein said length corresponds to a length of a posterior annulus.
6. The implant of claim 1 , wherein the length is within the range of from about 0.5 cm to about 3 cm.
7. The implant of claim 1 , wherein the height is within the range of from about 0.2 cm to about 1.5 cm.
8. The implant of claim 1 , wherein at least a portion of the implant is operable to resist or promote tissue ingrowth.
9. The implant of claim 1 , wherein said thickness is in the range of 0.127 mm to 1.600 mm.
10. The implant of claim 1 , wherein said thickness is in the range of 0.0762 mm to 0.381 mm.
11. The implant of claim 1 , wherein said barrier prevents the flow of all endogenous or prosthetic material beyond said barrier along said longitudinal axis.
12. The implant of claim 1 , wherein said barrier completely prevents the passage of said material around the barrier.
13. The implant of claim 1 , wherein said barrier prevents the passage of said material around either side of the barrier and beyond said barrier.
14. An implant for reinforcing an annulus of an intervertebral disc, comprising:
a support member having a first surface for placement against an interior surface of an annulus lamella and a second opposing surface, wherein said support member is adapted to be sealably positioned against the lamella via the exertion of force on at least a portion of the second surface sustained by a pressurized intervertebral disc environment;
wherein the support member has a length that is oriented along the circumference of the disc and a height that is oriented along the distance separating the surrounding vertebral bodies;
wherein said length is greater than said height;
wherein the implant is concave along at least a portion of said first surface and convex along at least a portion of said second surface; and
wherein the support member has a pre-formed concavity and is thereby inherently concave along at least a portion of said length;
wherein the support member comprises a membrane and a metal latticed frame that expands the membrane, wherein the frame contacts a substantial portion of the membrane and centrally supports the membrane; and
wherein a natural flow or egress of material from the nucleus to the anulus occurs along a longitudinal axis, wherein said longitudinal access is parallel to the height of said support member;
wherein said material comprises endogenous nucleus pulposus or prosthetic augmentation material;
wherein said support member has a thickness in a range of about 0.025 mm to about 2.5 mm;
wherein said support member provides a seal and comprises a rigidity that prevents the natural flow or egress of material beyond said support member along said longitudinal axis;
wherein said support member closes or barricades the area to be sealed to recreate the closed isobaric environment of a healthy disc nucleus.
15. An implant for reinforcing an annulus of an intervertebral disc, comprising:
a support member having a first surface for placement against an interior surface of an annulus lamella and a second opposing surface, wherein said support member is adapted to be sealably positioned against the lamella via the exertion of force on at least a portion of the second surface sustained by a pressurized intervertebral disc environment;
wherein the support member has a length that is oriented along the circumference of the disc and a height that is oriented along the distance separating the surrounding vertebral bodies;
wherein said length is greater than said height;
wherein said length and said height are dimensioned to prevent the barrier from slipping after insertion in the intervertebral disc;
wherein the support member has a pre-formed concavity and is thereby inherently concave along at least a portion of said length;
wherein the support member comprises a membrane and a sheet-like frame that expands the membrane, wherein the frame contacts a substantial portion of the membrane and supports at least the central portion of said membrane; and
wherein a natural flow or egress of material from the nucleus to the anulus occurs along a longitudinal axis, wherein said longitudinal access is parallel to the height of said support member;
wherein said material comprises endogenous nucleus pulposus or prosthetic augmentation material;
wherein said support member has a thickness in a range of about 0.025 mm to about 2.5 mm;
wherein said support member provides a seal and comprises a rigidity that prevents natural flow or egress of material beyond said support member along said longitudinal axis; and
wherein said support member closes or barricades the area to be sealed.
16. An implant for reinforcing an annulus of an intervertebral disc, comprising:
a support member having a first surface for placement against an interior surface of an annulus lamella and a second opposing surface, wherein said support member is adapted to be sealably positioned against the lamella via the exertion of force on at least a portion of the second surface sustained by a pressurized intervertebral disc environment;
wherein the support member has a length that is oriented along the circumference of the disc and a height that is oriented along the distance separating the surrounding vertebral bodies;
wherein said length is greater than said height;
wherein said length and said height are dimensioned to distribute pressure along the annulus;
wherein the support member has a pre-formed concavity and is thereby inherently concave along at least a portion of said length;
wherein the support member comprises a membrane and a sheet-like latticed enlarging means that expands the membrane, wherein the enlarging means contacts a substantial portion of the membrane and supports at least the central portion of said membrane; and
wherein a natural flow or egress of material from the nucleus to the anulus occurs along a longitudinal axis, wherein said longitudinal access is parallel to the height of said support member;
wherein said material comprises endogenous nucleus pulposus or prosthetic augmentation material;
wherein said support member has a thickness in a range of about 0.025 mm to about 2.5 mm;
wherein said support member provides a seal and comprises a rigidity that prevents natural flow or egress of material beyond said support member along said longitudinal axis; and
wherein said support member closes or barricades the area to be sealed.
17. An implant for reinforcing an annulus of an intervertebral disc, comprising:
a support member having a first surface for placement against an interior surface of an annulus lamella and a second opposing surface, wherein said support member is adapted to be sealably positioned against the lamella via the exertion of force on at least a portion of the second surface sustained by a pressurized intervertebral disc environment;
wherein the support member has a length that is oriented along the circumference of the disc and a height that is oriented along the distance separating the surrounding vertebral bodies;
wherein said length is greater than said height;
wherein the implant is concave along at least a portion of said length; and
wherein the support member has a pre-formed concavity and is thereby inherently concave along at least a portion of said length;
wherein the support member comprises a membrane and a sheet-like metallic enlarging means that expands the membrane, wherein the enlarging means contacts a substantial portion of the membrane and supports at least the central portion of said membrane; and
wherein a natural flow or egress of material from the nucleus to the anulus occurs along a longitudinal axis, wherein said longitudinal access is parallel to the height of said support member;
wherein said material comprises endogenous nucleus pulposus or prosthetic augmentation material;
wherein said support member has a thickness in a range of about 0.025 mm to about 2.5 mm;
wherein said support member provides a seal and comprises a rigidity that prevents natural flow or egress of material beyond said support member along said longitudinal axis; and
wherein said support member closes or barricades the area to be sealed.