FDA 510(k) Applications Submitted by COGENT SPINE LLC

FDA 510(k) Number Submission Date Device Name Applicant
K151406 05/26/2015 Cogent Lateral Interbody System COGENT SPINE LLC
K142193 08/11/2014 COGENT MED-LIF XL COGENT SPINE LLC
K132738 09/03/2013 COGENT MED-LIF COGENT SPINE LLC


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