Biopro, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2017-09-14
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K163627 | Shotel Ankle Arthrodesis Nail System | HSB | 2017-09-14 | View |
| 510(k) | K162674 | BioPro Foot Plating Systems | HRS | 2017-06-16 | View |
No matching devices.