Genesis Fracture Care, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2017-10-23
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K171293 | G3™ Active Plate® Miniature System | HRS | 2017-10-23 | View |
| 510(k) | K160633 | G3(TM) Active Plate(R) Small Fragment System | HRS | 2016-04-22 | View |
No matching devices.