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: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Avitus Orthopaedics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Keystone Regulatory Services, LLC as regulatory consultant.
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