Codman and Shurtleff, Inc. is one of 19683 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Codman and Shurtleff, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DELTAMAXX 18 MICROCOIL SYSTEM
1
Total
1
Cleared
0
Denied
Codman and Shurtleff, Inc. has 1 FDA 510(k) cleared medical devices. Based in Raynham, US.
Historical record: 1 cleared submissions from 2012 to 2012. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Codman and Shurtleff, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Codman and Shurtleff, Inc.
1 devices