Osteomed
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K203479 | ExtremiLOCK Lateral Ankle Fusion Plates | HRS | 2021-02-24 | View |
| 510(k) | K162542 | OsteoMed PINNACLE Driver | HBE | 2017-05-19 | View |
| 510(k) | K162544 | OsteoMed PINNACLE Driver | KMW | 2017-04-04 | View |
| 510(k) | K161041 | OsteoMed ExtremiLOCK Wrist Plating System | HRS | 2016-05-19 | View |
| 510(k) | K131851 | OSTEOMED NEURO RONGEUR | HAE | 2013-12-06 | View |
| 510(k) | K133437 | 1ST MTP PLATE | HRS | 2013-12-02 | View |
| 510(k) | K130412 | OSTEOMED EXTREMIFUSE SYSTEM | HWC | 2013-05-31 | View |
| 510(k) | K121304 | OSTEOMED CRANIAL DISTRACTION SYSTEM | PBJ | 2012-08-22 | View |
No matching devices.
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