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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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