Keos
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories2
Latest FDA decision2022-06-06
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K212450 | Keos Anterior Cervical Interbody Fusion Device System | ODP | 2022-06-06 | View |
| 510(k) | K193174 | Keos Lumbar IBFD | MAX | 2019-12-16 | View |
| 510(k) | K163386 | Keos Lumbar IBFD | MAX | 2017-04-10 | View |
| 510(k) | K160631 | Keos Lumbar IBFD | MAX | 2016-07-15 | View |
No matching devices.