Rebound Therapeutics Corporation
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest Approval2023-10-27
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K232618 | Aurora Surgiscope System | GWG | 2023-10-27 | View |
| 510(k) | K182211 | Aurora Surgiscope System | GWG | 2019-01-18 | View |
No matching devices.