Curiteva, LLC
FDA 510(k) & PMA Approved Devices — 4 products
Total Devices4
Categories3
Latest Approval2018-12-20
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K181589 | Curiteva Lumbar Interbody Fusion System | MAX | 2018-12-20 | View |
| 510(k) | K181549 | Curiteva Midline Anterior Cervical Plate System (or Curiteva Anterior Cervical Plate System) | KWQ | 2018-08-03 | View |
| 510(k) | K181562 | Curiteva Anterior Cervical Plate System | KWQ | 2018-08-02 | View |
| 510(k) | K181261 | Curiteva Cervical Interbody Fusion System | ODP | 2018-07-09 | View |
No matching devices.