Acuitive Technologies
Acuitive Technologies appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Nov 6, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K240450 | Citrepore | Nov 6, 2024 |
| K232592 | CITRELOCK® DUO | Sep 20, 2023 |
| K221468 | Citregen Tendon Interference Screw (TIS), Citrelock Tendon Fixation Device, Citrespline and Citre | Feb 14, 2023 |
| K220833 | Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACL | Nov 4, 2022 |
| K210239 | CITRESPLINE and CITRELOCK ACL Implants | Feb 24, 2021 |
| K203334 | The Citrefix Knotless Suture Anchor | Feb 5, 2021 |
| K200725 | Citregen Tendon Interference Screw and Citrelock | Oct 7, 2020 |