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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 Size Type Device Class Implantable

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CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heights. All CAVUX™ Cervical Cage-L implants are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are provided sterile and are single-use only.
Providence Medical Technology, Inc.
PD-31-612
In Commercial Distribution

  • 10852776006369 ()
  • 00852776006362 ()
PD-31-612

  • Implantable cervical facet joint distractor
CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heights. All CAVUX™ Cervical Cage-L implants are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are provided sterile and are single-use only.
Providence Medical Technology, Inc.
PD-31-611
In Commercial Distribution

  • 10852776006352 ()
  • 00852776006355 ()
PD-31-611

  • Implantable cervical facet joint distractor
CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heights. All CAVUX™ Cervical Cage-L implants are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are provided sterile and are single-use only.
Providence Medical Technology, Inc.
PD-31-610
In Commercial Distribution

  • 10852776006345 ()
  • 00852776006348 ()
PD-31-610

  • Implantable cervical facet joint distractor
CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heights. All CAVUX™ Cervical Cage-L implants are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are provided sterile and are single-use only.
Providence Medical Technology, Inc.
PD-31-609
In Commercial Distribution

  • 00852776006331 ()
  • 10852776006338 ()
PD-31-609

  • Implantable cervical facet joint distractor
CAVUXTM Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system.
Providence Medical Technology, Inc.
PD-31-604
In Commercial Distribution

  • 10852776006291 ()
  • 00852776006294 ()
PD-31-604

  • Implantable cervical facet joint distractor
CAVUX Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system.
Providence Medical Technology, Inc.
PD-31-603
In Commercial Distribution

  • 10852776006284 ()
  • 00852776006287 ()
PD-31-603

  • Implantable cervical facet joint distractor
CAVUX Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system.
Providence Medical Technology, Inc.
PD-31-601
In Commercial Distribution

  • 10852776006260 ()
  • 00852776006263 ()
PD-31-601

  • Implantable cervical facet joint distractor
CAVUXTM Cervical Cage is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine (C3-C7) with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have received at least six weeks of non-operative treatment prior to treatment with the device. Devices are intended to be used with autogenous bone graft and supplemental fixation, such as an anterior plating system.
Providence Medical Technology, Inc.
PD-31-600
In Commercial Distribution

  • 10852776006253 ()
  • 00852776006256 ()
PD-31-600

  • Implantable cervical facet joint distractor
The ALLY Bone Screw is a single-use implant made of titanium alloy and used in bone reconstruction, osteotomy, arthrodesis, join fusion, fracture repair and fixation appropriate for the size of the device.
Providence Medical Technology, Inc.
PD-32-301
In Commercial Distribution

  • 00852776006027 ()
PD-32-301

  • Implantable cervical facet joint distractor
The DTRAX Bone Screw is a single-use implant made of titanium alloy and used in bone reconstruction, osteotomy, arthrodesis, join fusion, fracture repair and fixation appropriate for the size of the device.
Providence Medical Technology, Inc.
PD-32-301
Not in Commercial Distribution

  • 10852776006024 ()
PD-32-301

  • Implantable cervical facet joint distractor
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