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.
FDA 510(k) cleared devices by Accufix Surgical, Inc.
2 devices