Ortho Kinematics, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
Total Devices3
Categories1
Latest FDA decision2017-11-08
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K173247 | Surgical Planning Software version 1.1 | LLZ | 2017-11-08 | View |
| 510(k) | K172327 | VMA™ System version 3.0 | LLZ | 2017-08-25 | View |
| 510(k) | K171617 | OKI Surgical Planning Software | LLZ | 2017-08-22 | View |
No matching devices.