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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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