Acuitive Technologies, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K240450 | Citrepore | November 6, 2024 |
| K232592 | CITRELOCK® DUO | September 20, 2023 |
| K221468 | Citregen Tendon Interference Screw (TIS), Citrelock Tendon Fixation Device, Citrespline and Citre | February 14, 2023 |
| K220833 | Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACL | November 4, 2022 |
| K210239 | CITRESPLINE and CITRELOCK ACL Implants | February 24, 2021 |
| K203334 | The Citrefix Knotless Suture Anchor | February 5, 2021 |
| K200725 | Citregen Tendon Interference Screw and Citrelock | October 7, 2020 |