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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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