FDA 510(k) Applications Submitted by BAILEY LIPSCOMB

FDA 510(k) Number Submission Date Device Name Applicant
K991364 04/20/1999 MODIFICATION TO TENOR SPINAL SYSTEM-PLATES SOFAMOR DANEK USA,INC.
K982686 08/03/1998 MODIFICATION TO TOWNLEY PEDICLE SCREW PLATING SYSTEM SOFAMOR DANEK USA,INC.
K992928 08/31/1999 CD HORIZON SPINAL SYSTEM SOFAMOR DANEK USA,INC.


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