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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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