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FDA 510(k) Applications Submitted by JAMIE WILSON
FDA 510(k) Number
Submission Date
Device Name
Applicant
K200613
03/09/2020
Tritanium« X TL Expandable Curved Posterior Lumbar Cage
Stryker Corporation
K161798
06/30/2016
FacetBRIDGE« System
LDR SPINE USA, INC.
K162133
08/01/2016
VerteFIT Corpectomy Cage System
LDR SPINE USA, INC.
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