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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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