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Interbody Fusion Device 7 Degree Standard 11mm
TITAN SPINE, LLC
2107-0111
Not in Commercial Distribution
- M682210701110 ()
- Lordotic Angle 7 Deg
- Height: 11 Millimeter
- Depth: 21 Millimeter
- Angle: 7 degree
- Width: 32 Millimeter
- width(MLxAP), 32 x 21, mm
2107-0111
- Metallic spinal interbody fusion cage
Interbody Fusion Device 7 Degree Standard 10mm
TITAN SPINE, LLC
2107-0110-S
Not in Commercial Distribution
- M68221070110S0 ()
- Lordotic Angle 7 Deg
- Height: 10 Millimeter
- Depth: 21 Millimeter
- width(MLxAP), 32 x 21, mm
- Width: 32 Millimeter
- Angle: 7 degree
2107-0110-S
- Metallic spinal interbody fusion cage
Interbody Fusion Device nanoLOCK Surface Technology 7 Degree Standard 10mm
TITAN SPINE, LLC
2107-0110-N
Not in Commercial Distribution
- M68221070110N0 ()
- Lordotic Angle 7 Deg
- Height: 10 Millimeter
- width(MLxAP), 32 x 21, mm
- Width: 32 Millimeter
- Angle: 7 degree
- Depth: 21 Millimeter
2107-0110-N
- Metallic spinal interbody fusion cage
Interbody Fusion Device 7 Degree Standard 10mm
TITAN SPINE, LLC
2107-0110
Not in Commercial Distribution
- M682210701100 ()
- Height: 10 Millimeter
- Lordotic Angle 7 Deg
- width(MLxAP), 32 x 21, mm
- Width: 32 Millimeter
- Angle: 7 degree
- Depth: 21 Millimeter
2107-0110
- Metallic spinal interbody fusion cage
VALEO Z 99x99mm x 99mm height 6º Lordosis, textured
AMEDICA CORPORATION
C
In Commercial Distribution
- M555999999999 ()
- Height: 99 Millimeter
11.009.1605
- Metallic spinal interbody fusion cage
18mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation.
MEDICAL DESIGNS LLC
11-9902-FD9
In Commercial Distribution
- 1199029 ()
- M364119902FD90 ()
- Outer Diameter: 18 Millimeter
- Length: 21 Millimeter
- Metallic spinal interbody fusion cage
16mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation.
MEDICAL DESIGNS LLC
11-9902-FD8
In Commercial Distribution
- 1199028 ()
- M364119902FD80 ()
- Outer Diameter: 16 Millimeter
- Length: 25 Millimeter
- Metallic spinal interbody fusion cage
16mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation.
MEDICAL DESIGNS LLC
11-9902-FD7
In Commercial Distribution
- M364119902FD70 ()
- Metallic spinal interbody fusion cage
14mm x 25mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation.
MEDICAL DESIGNS LLC
11-9902-FD6
In Commercial Distribution
- 1199026 ()
- M364119902FD60 ()
- Outer Diameter: 14 Millimeter
- Length: 25 Millimeter
- Metallic spinal interbody fusion cage
14mm x 21mm Cage; The Asfora Bullet Cage® is indicated for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) and instability in the lumbar spine at one or two contiguous levels from L2 to S1. DDD for lumbar systems is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. The DDD patients may also have up to Grade I spondylolisthesis at the involved level(s). The ABC cage devices are used with autogenous bone graft. Patients should be skeletally mature and have had at least six (6) months of non-operative treatment prior to implant. When implanted via a posterior (PLIF, TLIF) approach, this device should be used with supplemental fixation.
MEDICAL DESIGNS LLC
11-9902-FD5
In Commercial Distribution
- 1199025 ()
- M364119902FD50 ()
- Outer Diameter: 14 Millimeter
- Length: 21 Millimeter
- Metallic spinal interbody fusion cage