Amedica Corp.
Contact: Robert Wolfarth
Web: http://www.amedicacorp.com
E-Mail:
Address: 1885 West 2100 South, Salt Lake City, Utah 84119, USA
Phone: +1-(801)-839-3500 | Fax: +1-(801)-839-3605 | Map/Directions >>
Profile: Amedica Corp. is engaged in the production of orthopedic implant products. Our products include compact VBR spacer, VBR lumbar spacer, cervical plate system, anterior cervical plate system, pedicle screw system and synthetic bone putty. Our Valeo® C compact VBR spacer is designed to restore the biomechanical integrity of the anterior, middle, and posterior spine for a prolonged period of times. Our Valeo® CP- cervical plate systems are designed to facilitate accurate placement of the cervical plate & ensure proper angling and single-step insertion of the screws into the vertebrae. Our Valeo® CP-interior cervical plate system is an anterior cervical plate that is intended for temporary stabilization of the cervical spine from C2-C7. We offer Valeo® PS-pedicle screw systems that are designed to minimize soft tissue interference and help to secure posterior graft materials. Our Valeo® BP-synthetic bone putty enables cell infiltration, wicking capability, blood vessel ingrowth and a controlled respiration rate to promote healings.
FDA Registration Number: 3005032068
14 Products/Services (Click for related suppliers)
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| • Anterior Cervical Fixation Systems |
| • Cervical Intervertebral Fusion Device With Bone Graft (FDA Code: ODP / 888.3080) |
| • Cervical Plate System |
| • Lumbar Intervertebral Fusion Device with Bone Graft (FDA Code: MAX / 888.3080) |
| • Lumbar Spacer Systems |
| • Orthopedic Manual Surgical Instrument (FDA Code: LXH / 888.4540) An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench. |
| • Pedicle Screw System |
| • Spinal Intervertebral Body Fixation Appliance (FDA Code: KWQ / 888.3060) A spinal intervertebral body fixation orthosis is a device intended to be implanted made of titanium. It consists of various vertebral plates that are punched into each of a series of vertebral bodies. An eye-type screw is inserted in a hole in the center of each of the plates. A braided cable is threaded through each eye-type screw. The cable is tightened with a tension device and it is fastened or crimped at each eye-type screw. The device is used to apply force to a series of vertebrae to correct "sway back," scoliosis (lateral curvature of the spine), or other conditions. |
| • Spinal Pedicle Fixation Orthosis (FDA Code: MNI / 888.3070) Pedicle screw spinal systems are multiple component devices, made from a variety of materials, including alloys such as 316L stainless steel, 316LVM stainless steel, 22Cr-13Ni-5Mn stainless steel, Ti-6Al-4V, and unalloyed titanium, that allow the surgeon to build an implant system to fit the patient's anatomical and physiological requirements. Such a spinal implant assembly consists of a combination of anchors (e.g., bolts, hooks, and/or screws); interconnection mechanisms incorporating nuts, screws, sleeves, or bolts; longitudinal members (e.g., plates, rods, and/or plate/rod combinations); and/or transverse connectors. |
| • Spinal Pedicle Fixation Orthosis For Degenerative Disc Disease (FDA Code: NKB / 888.3070) |
| • Spinal Spacers |
| • Spinal Vertebral Body Replacement Device (FDA Code: MQP / 888.3060) |
| • Spondylolisthesis Spinal Fixation Orthosis (FDA Code: MNH / 888.3070) |
| • Synthetic Bone Putties |
