Orthofix Medical Inc. products

The M6-C artificial cervical disc is the natural choice for helping preserve motion in patients undergoing cervical disc replacement. Designed to mimic the structure and movement of a patient’s natural vertebral disc, the M6-C disc is the only artificial disc that incorporates an artificial nucleus and woven fiber annulus. The M6-C disc offers an innovative non-fusion solution in treating degeneration of the cervical disc. 

The PhysioStim device provides a safe, non-invasive option for treating fractures that are difficult to heal. With an overall clinical success rate of 80 percent (up to 88 percent for fracture gaps less than 3mm), PhysioStim devices have high success rates for treating nonunion fractures. The device assists in fracture healing by delivering a pulsed electromagnetic field (PEMF) signal to the targeted fracture site.

The Centurion Posterior Occipital Cervico-Thoracic (POCT) System is a temporary, multiple component system comprised of a variety of non-sterile, single use components made of titanium alloy or cobalt chrome alloy that allow the surgeon to build a spinal implant construct. The Centurion POCT System consists of an assortment of rods, set screws, axial connectors, lateral offset adapters, multi-axial screws, cross connectors, hooks, plates, bone screws, and cables (titanium).

CETRA is a new ACP system designed to meet the needs of today’s surgeon. The system offers a variety of options to fit patient anatomy and provide precise fixation delivery. CETRA consists of quality instruments and implants that are cost effective and designed to simplify and reduce surgical time. The plate features large graft windows that give the surgeon better visualization of the disc space while the plate is in place. CETRA also includes a single step locking mechanism that does not require a torque driver and can be locked with the same driver that is used to drive the bone screws. This system gives surgeons a wide range of screw options to best suit each patient and achieve up to 20 degrees of screw angulation.

The CONSTRUX Mini PEEK Spacer System is comprised of a variety of implants manufactured from PEEK in two footprint sizes, small and large, and in various heights, in one-millimeter increments. The superior and inferior surfaces of the implant have a pattern of ripples to provide increased stability and help prevent anterior/posterior movement of the device.

The Trinity ELITE allograft, a third generation allograft with viable cells, provides a unique alternative to autograft, long considered the standard for bone grafting. Exclusively processed for Orthofix by our premier partner, MTF Biologics, the Trinity ELITE allograft builds on the exemplary safety profile of more than 200,000 Trinity Evolution and Trinity ELITE allograft procedures to date. 

The Trinity Evolution allograft is comprised of cancellous bone with viable osteogenic and osteoprogenitor cells retained within the matrix and a demineralized cortical bone component. The Trinity Evolution allograft offers an ideal alternative to autograft and other bone grafting options.

The VersaShield amniotic membrane is designed to serve as a wound covering and protective barrier for a variety of surgical demands.

The CervicalStim device is the only bone growth stimulation therapy approved by the FDA as a noninvasive, adjunctive treatment option for cervical fusion in patients at high-risk for non-fusion. The device uses a pulsed electromagnetic field (PEMF) to induce a low-level electrical field at the fusion site which stimulates bone healing at a molecular, cellular, and tissue level. With an overall clinical success rate of 84 percent, the CervicalStim device increases fusion success significantly by 22 percent when used adjunctively to surgery.

The SpinalStim device is FDA approved to be used after spinal fusion surgery or to be used to treat a failed fusion from a previous surgery. The devices stimulate the natural healing process of bone by sending low-level pulses of electromagnetic energy to the injury or fusion site. The device has an overall clinical success rate of 92% in treating spinal fusion surgery patients. In addition, the SpinalStim device can be used for treatment of a failed spinal fusion, reducing the need for a revision surgery.