Whitmore Ent., Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K933778 | WHITMORE ANKLE X-RAY EXTENSION (AXE) | KPR | 1993-12-13 | View |
| 510(k) | K931037 | WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100) | FWZ | 1993-07-30 | View |
No matching devices.
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