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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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