Accufix Surgical, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Accufix Surgical, Inc. has 2 FDA 510(k) cleared medical devices. Based in West Haven, US.
Latest FDA clearance: Feb 2024. Active since 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Accufix Surgical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Technologies as regulatory consultant.
2 devices