OrthoPediatrics Receives FDA Clearance for ResponseTM Spine System

Warsaw, Indiana, June 1, 2015 – OrthoPediatrics Corp. announced it has received 510(k) clearance from the U.S. Food and Drug Administration to market the ResponseTM Spine System. This system is intended for posterior, non-cervical fixation (pedicle screw fixation T1-S2/ilium and hook fixation T1-L5) in pediatric patients is indicated as an adjunct to fusion to treat Adolescent Idiopathic Scoliosis. The device is intended to be used with autograph and/or allograft.
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