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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