Avitus Orthopaedics, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Avitus Orthopaedics, Inc. has 5 FDA 510(k) cleared medical devices. Based in Farmington, US.
Last cleared in 2023. Active since 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Avitus Orthopaedics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Avitus Orthopaedics, Inc.
5 devices
Cleared
Jul 17, 2023
Avitus® DragonWing Large Volume Autograft Delivery System
Orthopedic
59d
Cleared
Jun 26, 2023
Avitus® Precision Autograft Delivery System
General & Plastic Surgery
123d
Cleared
Mar 31, 2021
Avitus(r) Bone Harvester
Orthopedic
28d
Cleared
Mar 20, 2017
Avitus Bone Harvester with Filter Insert - 5mm, Avitus Bone Harvester - 5mm,...
Gastroenterology & Urology
25d
Cleared
Oct 23, 2015
Avitus Bone Harvester
Gastroenterology & Urology
53d