Genesis Orthopedics, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Advertisement
Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K954511 | GO INTRAMEDULLARY NAIL LOCKING SCREW | HWC | 1995-12-19 | View |
| 510(k) | K954543 | GO UNIVERSALK-WIRE FLUTED DRILL | HTY | 1995-12-08 | View |
No matching devices.
Advertisement