Shanghai Iatrical-Ti Technologies CO , Ltd.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest Approval2024-09-06
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K232996 | Iatrical Interbody Lumbar Fusion Systems (Model ALIF, Model TLIF, Model LLIF) | MAX | 2024-09-06 | View |
No matching devices.