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OLIF II Trial
GS Medical Co., Ltd.
GS132-3608P
In Commercial Distribution
- 08809974806104 ()
GS132-3608P
- Polymeric spinal interbody fusion cage
The Pulsar Expandable PLIF Cage devices are designed for restoring the height of the intervertebral space after resection of the disc. The Pulsar Expandable PLIF Cage devices consist of implants in various heights, footprints, and lordotic configurations with architecture designed to accept pre and post packing of bone graft material. The intervertebral body devices are made of titanium alloy (Ti-6AL-4V ELI). The Pulsar Expandable PLIF Cage devices are not radio lucent, but have large windows through the sides that will allow visualization of the placement and subsequent bone fusion. The Expandable PLIF Cage (Posterior Lumbar Interbody Fusion Cage) are designed for segments L2 to S1.
GS Medical Co., Ltd.
2212-1085
In Commercial Distribution
- 08809974803974 ()
2212-1085
- Polymeric spinal interbody fusion cage
The Pulsar Expandable PLIF Cage devices are designed for restoring the height of the intervertebral space after resection of the disc. The Pulsar Expandable PLIF Cage devices consist of implants in various heights, footprints, and lordotic configurations with architecture designed to accept pre and post packing of bone graft material. The intervertebral body devices are made of titanium alloy (Ti-6AL-4V ELI). The Pulsar Expandable PLIF Cage devices are not radio lucent, but have large windows through the sides that will allow visualization of the placement and subsequent bone fusion. The Expandable PLIF Cage (Posterior Lumbar Interbody Fusion Cage) are designed for segments L2 to S1.
GS Medical Co., Ltd.
2212-1081
In Commercial Distribution
- 08809974803967 ()
2212-1081
- Polymeric spinal interbody fusion cage
The Pulsar Expandable PLIF Cage devices are designed for restoring the height of the intervertebral space after resection of the disc. The Pulsar Expandable PLIF Cage devices consist of implants in various heights, footprints, and lordotic configurations with architecture designed to accept pre and post packing of bone graft material. The intervertebral body devices are made of titanium alloy (Ti-6AL-4V ELI). The Pulsar Expandable PLIF Cage devices are not radio lucent, but have large windows through the sides that will allow visualization of the placement and subsequent bone fusion. The Expandable PLIF Cage (Posterior Lumbar Interbody Fusion Cage) are designed for segments L2 to S1.
GS Medical Co., Ltd.
2212-1080
In Commercial Distribution
- 08809974803950 ()
2212-1080
- 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.
2210-0847
In Commercial Distribution
- 08809974803882 ()
2210-0847
- 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.
2210-0744
In Commercial Distribution
- 08809974803868 ()
2210-0744
- Polymeric spinal interbody fusion cage
SA ACIF Cage Caddy
GS Medical Co., Ltd.
GS136-9667
In Commercial Distribution
- 08809974799840 ()
GS136-9667
- Polymeric spinal interbody fusion cage
SA ACIF Cage Caddy
GS Medical Co., Ltd.
GS136-9666
In Commercial Distribution
- 08809974799833 ()
GS136-9666
- Polymeric spinal interbody fusion cage
DL Nav Compatible Tap Ø8.5
GS Medical Co., Ltd.
GS110-5063
In Commercial Distribution
- 08809974799826 ()
GS110-5063
- Polymeric spinal interbody fusion cage
DL Nav Compatible Tap Ø7.5
GS Medical Co., Ltd.
GS110-5061
In Commercial Distribution
- 08809974799819 ()
GS110-5061
- Polymeric spinal interbody fusion cage