Amplify Surgical, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2022-10-18
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K222203 | DualXSLIM(R) T/PLIF | MAX | 2022-10-18 | View |
| 510(k) | K211740 | DualX | MAX | 2021-09-29 | View |
| 510(k) | K192434 | DualX Lumbar Intervertebral Body Fusion Device | MAX | 2019-10-15 | View |
No matching devices.