FDA 510(k) Applications Submitted by SOUTHERN SPINE, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K130948 04/05/2013 C-FUSE CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM SOUTHERN SPINE, LLC
K123093 10/02/2012 STABILINK MIS SPINAL FIXATION SYSTEM SOUTHERN SPINE, LLC
K063764 12/20/2006 SOUTHERN SPINE ANTERIOR CERVICAL STABILIZATION SYSTEM, KWIK- FIX CERVICAL SYSTEM, AND KWIK-FIX / TS CERVICAL SYSTEM SOUTHERN SPINE, LLC


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