FDA 510(k) Applications Submitted by ORTHOFIX

FDA 510(k) Number Submission Date Device Name Applicant
K130176 01/25/2013 FIREBIRD SPINAL FIXATION SYSTEM ORTHOFIX
K122901 09/21/2012 FIREBIRD SPINAL FIXATION SYSTEM, PHOENIX MIS SPINAL FIXATION SYSTEM ORTHOFIX
K121649 06/05/2012 CONSTRUX MINI PEEK TI SPACER SYSTEM ORTHOFIX


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