Ceremed , Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2016-09-27
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K161446 | Biopor Porous Polyethylene Implants | GWO | 2016-09-27 | View |
| 510(k) | K160988 | Biopor, AOC Porous Polyethylene, Cerepor | KKY | 2016-07-14 | View |
No matching devices.