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FDA 510(k) Applications Submitted by WILLIAM SANDUL
FDA 510(k) Number
Submission Date
Device Name
Applicant
K100888
03/30/2010
MODIFICATION TO LANX POSTERIOR CERVICOTHORACIC SPINAL FIXATION SYSTEM
LANX, INC.
K121316
05/02/2012
LANX SPINAL FIZATION SYSTEM
LANX, INC.
K103660
12/15/2010
LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM
LANX, INC.
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