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) cleared devices by Medtronic Sofamor Danek USA,...
2 devices