FDA 510(k) Applications Submitted by SPINEWORKS, LLC

FDA 510(k) Number Submission Date Device Name Applicant
K111166 04/26/2011 A-WEDGE ANTERIOR INTERBODY SYSTEM (A-WEDGE A.I.S.) SPINEWORKS, LLC
K081331 05/12/2008 FIXXSURE CROSS LINK SPINEWORKS, LLC
K042600 09/23/2004 STANSION MATRIX SPINEWORKS, LLC
K133340 10/30/2013 SPINEWORKS ANTERIOR LUMBAR DEVICE SPINEWORKS, LLC


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