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FDA 510(k) Applications Submitted by SULZER SPINE-TECH
FDA 510(k) Number
Submission Date
Device Name
Applicant
K020344
02/01/2002
RPX TITANIUM CEMNT RESTRICTOR
SULZER SPINE-TECH
K992276
07/07/1999
MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEM
SULZER SPINE-TECH
K012305
07/23/2001
MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM
SULZER SPINE-TECH
K993067
09/13/1999
SILHOUETTE SPINAL FIXATION SYSTEM
SULZER SPINE-TECH
K020196
01/22/2002
MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEM
SULZER SPINE-TECH
K012173
07/12/2001
DEVICE MODIFICATION OF SILHOUETTE SPINDAL FIXATION SYSTEM
SULZER SPINE-TECH
K022374
07/22/2002
CADENCE SPINAL FIXATION SYSTEM
SULZER SPINE-TECH
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