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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