FDA 510(k) Applications Submitted by ADVANCED SPINE FIXATION SYSTEMS, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K990845 03/15/1999 MODIFICATION TO PARTS NUMBERED CGT-SL AND CGT-SL-15 ADVANCED SPINE FIXATION SYSTEMS, INC.
K992012 06/15/1999 WILTSE SYSTEM ADVANCED SPINE FIXATION SYSTEMS, INC.
K954770 10/17/1995 CENTRA-LINE GRAPPLE, VARIFIX SYSTEM ADVANCED SPINE FIXATION SYSTEMS, INC.


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