FDA 510(k) Applications Submitted by Acuitive Technologies, Inc.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K210239 |
01/29/2021 |
CITRESPLINE and CITRELOCK ACL Implants |
Acuitive Technologies, Inc. |
K220833 |
03/22/2022 |
Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACL |
Acuitive Technologies, Inc. |
K221468 |
05/20/2022 |
CitregenÖ Tendon Interference Screw (TIS), CitrelockÖ Tendon Fixation Device, CitresplineÖ and CitrelockÖ ACL Implants |
Acuitive Technologies, Inc. |
K232592 |
08/25/2023 |
CITRELOCK« DUO |
Acuitive Technologies, Inc. |
K203334 |
11/12/2020 |
The Citrefix Knotless Suture Anchor |
Acuitive Technologies, Inc. |
|
|