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PROVIDENCE MEDICAL TECHNOLOGY, INC.
PD-31-203
In Commercial Distribution
- 00852776006492 ()
- 10852776006499 ()
PD-31-203
- Metallic spinal interbody fusion cage
CAVUX® Cervical Cages are titanium constructs offered in various footprints and heights. All CAVUX® Cervical Cages are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are single-use only.
PROVIDENCE MEDICAL TECHNOLOGY, INC.
PD-31-202
In Commercial Distribution
- 00852776006423 ()
- 10852776006420 ()
- Metallic spinal interbody fusion cage
CAVUX® Cervical Cages are titanium constructs offered in various footprints and heights. All CAVUX Cervical Cages are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are single-use only.
PROVIDENCE MEDICAL TECHNOLOGY, INC.
PD-31-220
In Commercial Distribution
- 00852776006386 ()
- 10852776006383 ()
- Metallic spinal interbody fusion cage
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-31-201
In Commercial Distribution
- 10852776006321 ()
- 00852776006324 ()
- Metallic spinal interbody fusion cage
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
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-31-602
In Commercial Distribution
- 10852776006277 ()
- 00852776006270 ()
PD-31-602
- Metallic spinal interbody fusion cage
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
ACIF HOLDER STOPPER TYPE
Corentec Co., Ltd
SI.C10.0010
In Commercial Distribution
- 08806373874192 ()
- Surgical implant/trial-implant/sizer holder, reusable