Relievant Medsystems, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest Approval2022-10-26
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K222281 | Intracept Intraosseous Nerve Ablation System | GXI | 2022-10-26 | View |
| 510(k) | K213836 | Intracept Intraosseous Nerve Ablation System | GXI | 2022-03-11 | View |
No matching devices.