Acuitive Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Citrepore™, CITRELOCK® DUO, Citregen™ Tendon Interference Screw (TIS), Citrelock™ Tendon Fixation Device, Citrespline™ and Citrelock™ ACL Implants
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Acuitive Technologies, Inc. Orthopedic ✕
6 devices
Cleared
Nov 06, 2024
Citrepore™
Orthopedic
265d
Cleared
Sep 20, 2023
CITRELOCK® DUO
Orthopedic
26d
Cleared
Feb 14, 2023
Citregen™ Tendon Interference Screw (TIS), Citrelock™ Tendon Fixation Device,...
Orthopedic
270d
Cleared
Nov 04, 2022
Citregen Tendon Interference Screw, Citrelock, Citrefix, Citrespline ACL, and...
Orthopedic
227d
Cleared
Feb 24, 2021
CITRESPLINE and CITRELOCK ACL Implants
Orthopedic
26d
Cleared
Feb 05, 2021
The Citrefix Knotless Suture Anchor
Orthopedic
85d