Konigsee Implantate GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Konigsee Implantate GmbH has 1 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Konigsee Implantate GmbH Filter by specialty or product code using the sidebar.
1 devices