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The Blustone Synergy Slate System is a cervical interbody fusion system comprised of parallel and 6° lordotic cages in two footprints with varying heights designed to accommodate patient anatomy, and may be implanted as a single device via an anterior approach.
BLUSTONE SYNERGY, LLC
1713-CL06
In Commercial Distribution
- 00810482030316 ()
- Height: 6 Millimeter
- Width: 13 Millimeter
- Length: 17 Millimeter
- Polymeric spinal interbody fusion cage
The Blustone Synergy Slate System is a cervical interbody fusion system comprised of parallel and 6° lordotic cages in two footprints with varying heights designed to accommodate patient anatomy, and may be implanted as a single device via an anterior approach.
BLUSTONE SYNERGY, LLC
1713-CL05
In Commercial Distribution
- 00810482030309 ()
- Height: 5 Millimeter
- Width: 13 Millimeter
- Length: 17 Millimeter
- Polymeric spinal interbody fusion cage
The Blustone Synergy Slate System is a cervical interbody fusion system comprised of parallel and 6° lordotic cages in two footprints with varying heights designed to accommodate patient anatomy, and may be implanted as a single device via an anterior approach.
BLUSTONE SYNERGY, LLC
1411-CL11
In Commercial Distribution
- 00810482030071 ()
- Height: 11 Millimeter
- Width: 11 Millimeter
- Length: 14 Millimeter
- Polymeric spinal interbody fusion cage
The Blustone Synergy Slate System is a cervical interbody fusion system comprised of parallel and 6° lordotic cages in two footprints with varying heights designed to accommodate patient anatomy, and may be implanted as a single device via an anterior approach.
BLUSTONE SYNERGY, LLC
1411-CL09
In Commercial Distribution
- 00810482030057 ()
- Height: 9 Millimeter
- Width: 11 Millimeter
- Length: 14 Millimeter
- Polymeric spinal interbody fusion cage
The Blustone Synergy Slate System is a cervical interbody fusion system comprised of parallel and 6° lordotic cages in two footprints with varying heights designed to accommodate patient anatomy, and may be implanted as a single device via an anterior approach.
BLUSTONE SYNERGY, LLC
1411-CL07
In Commercial Distribution
- 00810482030033 ()
- Height: 7 Millimeter
- Width: 11 Millimeter
- Length: 14 Millimeter
- Polymeric spinal interbody fusion cage
The Blustone Synergy Slate System is a cervical interbody fusion system comprised of parallel and 6° lordotic cages in two footprints with varying heights designed to accommodate patient anatomy, and may be implanted as a single device via an anterior approach.
BLUSTONE SYNERGY, LLC
1411-CL05
In Commercial Distribution
- 00810482030019 ()
- Height: 5 Millimeter
- Width: 11 Millimeter
- Length: 14 Millimeter
- Polymeric spinal interbody fusion cage
"The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560).
The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine."
GS Medical Co., Ltd.
1144-0714
In Commercial Distribution
- 08806162106213 ()
1144-0714
- Polymeric spinal interbody fusion cage
"The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560).
The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine."
GS Medical Co., Ltd.
1144-0711
In Commercial Distribution
- 08806162106183 ()
1144-0711
- Polymeric spinal interbody fusion cage
"The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560).
The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine."
GS Medical Co., Ltd.
1144-0709
In Commercial Distribution
- 08806162106169 ()
1144-0709
- Polymeric spinal interbody fusion cage
"The GS Medical AnyPlus PEEK Lumbar Cage device consists of implants available in various heights and lordotic configurations with an open architecture to accept packing of bone graft material. The implants are made of polyether-ether-ketone (PEEK OPTIMA LT1) (Manufacturer – INVIBIO) body (PEEK conforming to ASTM F2026) with the x-ray markers made of Tantulum (conforming to ASTM F560).
The AnyPlus PEEK Lumbar Cage is indicated for use with autogenous bone graft in skeletally mature patients with degenerative disc disease (""DDD"") at one or two contiguous spinal levels from L2-S1. DDD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level(s). The AnyPlus PEEK Lumbar Cage is to be combined with internal supplemental fixation cleared for use in the lumbar spine."
GS Medical Co., Ltd.
1144-0708
In Commercial Distribution
- 08806162106152 ()
1144-0708
- Polymeric spinal interbody fusion cage