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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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