Acuitive Technologies, Inc.
Acuitive Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2021, most recent 2024.
Top product codes for Acuitive Technologies, Inc.
Recent clearances by Acuitive Technologies, Inc.
- K240450 — Citrepore
- K232592 — CITRELOCK® DUO
- K221468 — Citregen Tendon Interference Screw (TIS), Citrelock Tendon Fixation Device, Citrespline and Citrelock ACL Implants
- K220833 — Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and Citrelock ACL
- K210239 — CITRESPLINE and CITRELOCK ACL Implants
- K203334 — The Citrefix Knotless Suture Anchor
Data sourced from openFDA. This site is unofficial and independent of the FDA.