Retropsoas Technologies, LLC
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2024-10-07
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K242457 | EARP Interbody System | MAX | 2024-10-07 | View |
| 510(k) | K241917 | EARP Nerve Cuff Electrode | ETN | 2024-07-31 | View |
No matching devices.