Medtronic Sofamor Danek USA, Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtronic Sofamor Danek USA, Incorporated - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Medtronic Sofamor Danek USA, Incorporated has 2 FDA 510(k) cleared medical devices. Based in Memphis, US.
Historical record: 2 cleared submissions from 2015 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Medtronic Sofamor Danek USA, Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medtronic Sofamor Danek USA, Incorporated
2 devices