Avanti Orthopaedics, Inc. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Avanti Orthopaedics, Inc. has 3 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Last cleared in 2022. Active since 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Avanti Orthopaedics, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Secure BioMed Evaluations as regulatory consultant.
3 devices