Circumfix Solutions, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Circumfix Solutions, Inc. - FDA 510(k) Cleared Devices
Recent clearances: VariTrax Sternal CircumFixation System
1
Total
1
Cleared
0
Denied
Circumfix Solutions, Inc. has 1 FDA 510(k) cleared medical devices. Based in Collierville, US.
Latest FDA clearance: Jan 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Circumfix Solutions, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by MRC Global as regulatory consultant.
FDA 510(k) Regulatory Record - Circumfix Solutions, Inc.
1 devices