Orthofix Medical, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest Approval2024-06-20
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K240830 | Reef TO/TA System; Regatta Lateral System; Explorer TO System; WaveForm C Interbody System; WaveForm TO Interbody System; WaveForm TA Interbody System; FORZA XP Expandable Spacer System; Shoreline ACS Interbody System; Shoreline RT Interbody System; Meridian Interbody System; WaveForm A Interbody System | MAX | 2024-06-20 | View |
No matching devices.