Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Acuitive Technologies, Inc.

FDA 510(k) & PMA Approved Devices — 6 products

Total Devices6
Categories3
Latest FDA decision2024-11-06
TypeNumberDevice NameCodeDateActions
510(k) K240450 Citrepore™MQV2024-11-06 View
510(k) K232592 CITRELOCK® DUOMBI2023-09-20 View
510(k) K221468 Citregen™ Tendon Interference Screw (TIS), Citrelock™ Tendon Fixation Device, Citrespline™ and Citrelock™ ACL ImplantsMAI2023-02-14 View
510(k) K220833 Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACLMAI2022-11-04 View
510(k) K210239 CITRESPLINE and CITRELOCK ACL ImplantsMAI2021-02-24 View
510(k) K203334 The Citrefix Knotless Suture AnchorMAI2021-02-05 View
↑