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Company also announces FDA clearance of latest addition to Salvation product portfolio.
March 25, 2015
By: Michael Barbella
Managing Editor
Most companies use the American Academy of Orthopedic Surgeons (AAOS) Annual Meeting to display their wares. Some strategically time new product releases or U.S. Food and Drug Administration (FDA) approvals to coincide with the event. And a select few do both. Wright Medical Group Inc. was one of the rare double-dippers at this year’s meeting, taking place March 24-28 in Las Vegas, Nev. The company kicked off the five-day show by announcing FDA approval of its Salvation External Fixation system, a product designed to address fractures, nonunions, and complex foot and ankle deformities including Charcot neuroarthropathy. Wright claims the system uses tensioned thin wires, half-pins, and rings to accomplish its goals, and incorporates various new features to help surgeons with proper frame positioning and increase frame application efficiency. The slotted ring design allows for frame components to be attached quickly and easily, while minimizing the need to assemble small, threaded components together, the company noted in a news release. The Salvation system includes components to assist in positioning the foot and lower leg within the frame and maintain an appropriate position throughout the surgery. In addition, the wire guide allows for precise placement of the wire on the ring to minimize the need for additional connection components and decrease additional surgical steps. The Salvation External Fixation System may be used for definitive treatment as the sole fixation device, or used in conjunction with the Salvation beams and bolts or the Salvation 3Di Midfoot Plating system. The Salvation External Fixation system is the latest addition to Wright’s Salvation Limb Salvage product portfolio, which includes the Salvation Beaming system and the Salvation 3Di Plating system. The portfolio is designed to address fractures, nonunions and complex foot and ankle deformities and is specifically indicated for neuropathic osteoarthropathy treatment (commonly referred to as Charcot foot), a deformity (most commonly mid-foot collapse) that results from nerve damage in the foot or ankle. Wright expects to initiate limited physician testing of the Salvation External Fixation system to collect market assessment data in the second quarter of 2015. The latest Salvation product was noticeably absent from Wright’s grandiose exhibit booth, but there was still plenty of innovations to behold, including:
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