Spine-Tech, Inc.
FDA 510(k) & PMA Approved Devices — 4 products
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Total Devices4
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K980288 | SPINE-TECH SILHOUETTE SPINAL FIXATION SYSTEM | KWP | 1998-07-29 | View |
| 510(k) | K970040 | SPINE-TECH BONE HARVESTER | HWE | 1997-02-28 | View |
| 510(k) | K951268 | SPINE-TECH MODIFIED LAPAROSCOPIC SPINAL FUSION INSTRUMENT SYSTEM | HRX | 1995-07-31 | View |
| 510(k) | K940913 | SPINE-TECH LAPAROSCOPIC INSTRUMENTATION SYSTEM | HRX | 1994-10-04 | View |
No matching devices.
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