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.


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