Acuitive Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 6 products
Total Devices6
Categories3
Latest Approval2024-11-06
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K240450 | Citrepore | MQV | 2024-11-06 | View |
| 510(k) | K232592 | CITRELOCK® DUO | MBI | 2023-09-20 | View |
| 510(k) | K221468 | Citregen Tendon Interference Screw (TIS), Citrelock Tendon Fixation Device, Citrespline and Citrelock ACL Implants | MAI | 2023-02-14 | View |
| 510(k) | K220833 | Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACL | MAI | 2022-11-04 | View |
| 510(k) | K210239 | CITRESPLINE and CITRELOCK ACL Implants | MAI | 2021-02-24 | View |
| 510(k) | K203334 | The Citrefix Knotless Suture Anchor | MAI | 2021-02-05 | View |
No matching devices.