Sulzer Spine-Tech
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K022374 | CADENCE SPINAL FIXATION SYSTEM | KWP | 2002-09-24 | View |
| 510(k) | K020344 | RPX TITANIUM CEMNT RESTRICTOR | JDK | 2002-05-02 | View |
| 510(k) | K020196 | MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEM | MNH | 2002-02-15 | View |
| 510(k) | K012173 | DEVICE MODIFICATION OF SILHOUETTE SPINDAL FIXATION SYSTEM | KWP | 2001-09-28 | View |
| 510(k) | K012305 | MODIFICATION TO: TRINICA ANTERIOR CERVICAL PLATE SYSTEM | KWQ | 2001-08-22 | View |
| 510(k) | K993067 | SILHOUETTE SPINAL FIXATION SYSTEM | KWP | 1999-11-16 | View |
| 510(k) | K992276 | MODIFICATION TO SILHOUETTE SPINAL FIXATION SYSTEM | MNI | 1999-10-01 | View |
No matching devices.
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