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

FDA 510(k) Number Submission Date Device Name Applicant
K120047 01/06/2012 CORAL SPINAL SYSTEM THEKEN SPINE, LLC
K120829 03/19/2012 STAINLESS STEEL SPINAL SYSTEM THEKEN SPINE, LLC
K121211 04/20/2012 VU APOD INTERVERTEBRAL BODY FUSION DEVICE THEKEN SPINE, LLC


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