Medtronic Sofamor Danck USA, Inc. - FDA 510(k) Cleared Devices
4
Total
3
Cleared
0
Denied
Medtronic Sofamor Danck USA, Inc. has 3 FDA 510(k) cleared medical devices. Based in Memphis, US.
Historical record: 3 cleared submissions from 2011 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Medtronic Sofamor Danck USA, Inc. Filter by specialty or product code using the sidebar.
4 devices