Coracoid Solutions, Inc. is one of 18450 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Coracoid Solutions, Inc. - FDA 510(k) Cleared Devices
Recent clearances: M-Fix Acromioclavicular Device
1
Total
1
Cleared
0
Denied
Coracoid Solutions, Inc. has 1 FDA 510(k) cleared medical devices. Based in Park City, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Coracoid Solutions, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Michael Kolber as regulatory consultant.
FDA 510(k) Regulatory Record - Coracoid Solutions, Inc.
1 devices