Orthonovis, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories3
Latest Approval2025-10-02
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K252758 | Cannulated Screw and Kirschner (K wire) System | HWC | 2025-10-02 | View |
| 510(k) | K250498 | BPS Wrist Fracture System | HRS | 2025-03-17 | View |
| 510(k) | K250055 | BPS - Bone Fragment Fixation Plates, Screws and Washers | HRS | 2025-02-06 | View |
| 510(k) | K242343 | BPS Wrist Fracture System | HRS | 2024-10-04 | View |
| 510(k) | K213905 | ONX Large External Fixation System | KTT | 2022-08-25 | View |
No matching devices.