Surgentec
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories2
Latest FDA decision2023-08-03
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K231831 | TiLink-L Joint Fusion System | OUR | 2023-08-03 | View |
| 510(k) | K201900 | 3D GraftRasp System | FMF | 2020-09-03 | View |
| 510(k) | K200431 | 3D GraftRasp System | FMF | 2020-05-18 | View |
No matching devices.