Profile: Vertebral Technologies, Inc. deals with interbody fusion systems and disc nucleus replacement systems. Our Interfuse™ interbody fusion system enables spine surgeons to achieve an ALIF-sized footprint through a familiar, less invasive, posterior approach. It helps spine surgeons solve a long standing dilemma and desire to perform less-invasive procedures on patients to minimize post operative pain, and to accelerate patient recovery times.
FDA Registration Number: 3007617183
7 Products/Services (Click for related suppliers)
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• Disc Nucleus Replacement Systems |
• Disc Replacements |
• Implantable Spinal Devices |
• Interbody Fusion Systems |
• Lumbar Intervertebral Fusion Device with Bone Graft (FDA Code: MAX / 888.3080) |
• Minimal Access Systems, Transforaminal Lumbar Interbody Fusion |
• 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. |