Osartis GmbH
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories2
Latest FDA decision2024-11-20
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K240856 | Hip Spacer Molds; Knee Spacer Molds; Shoulder Spacer Molds | MBB | 2024-11-20 | View |
| 510(k) | K202458 | BonOs Inject, Pedicle screw kits, Cement pusher | LOD | 2021-05-18 | View |
| 510(k) | K210120 | BonOs HV, BonOs MV, BonOs LV | LOD | 2021-03-19 | View |
| 510(k) | K210125 | BonOs HV Genta, BonOs MV Genta, BonOs LV Genta | LOD | 2021-03-19 | View |
| 510(k) | K192394 | Hi-Fatigue Bone Cement | LOD | 2019-12-02 | View |
| 510(k) | K192379 | Hi-Fatigue G Bone Cement | LOD | 2019-11-27 | View |
No matching devices.