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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Class Implantable

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Anyplus II Rod Pusher (Straight Type)
GS Medical Co., Ltd.
GS120-1710
In Commercial Distribution

  • 08800104099878 ()
GS120-1710

  • Polymeric spinal interbody fusion cage
Anyplus II Cannulated Poly Reduction Screw Driver
GS Medical Co., Ltd.
GS120-0950
In Commercial Distribution

  • 08800104099847 ()
GS120-0950

  • Polymeric spinal interbody fusion cage
Anyplus II Set Screw Final Driver, 12N
GS Medical Co., Ltd.
GS120-2400
In Commercial Distribution

  • 08800104099731 ()
GS120-2400

  • Polymeric spinal interbody fusion cage
Anyplus II Head Adjuster
GS Medical Co., Ltd.
GS120-3000
In Commercial Distribution

  • 08800104097973 ()
GS120-3000

  • Polymeric spinal interbody fusion cage
Anyplus II Set Screw Starter, Dual
GS Medical Co., Ltd.
GS120-2300
In Commercial Distribution

  • 08800104097959 ()
GS120-2300

  • 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.
8071-0007S
In Commercial Distribution

  • 08800104089978 ()
8071-0007S

  • 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.
2212-1181
In Commercial Distribution

  • 08800104089954 ()
2212-1181

  • 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.
2212-1180
In Commercial Distribution

  • 08800104089947 ()
2212-1180

  • 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.
2212-1111
In Commercial Distribution

  • 08800104089923 ()
2212-1111

  • 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.
2212-0985
In Commercial Distribution

  • 08800104089909 ()
2212-0985

  • Polymeric spinal interbody fusion cage
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