K2m, Incorporated is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
K2m, Incorporated - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
K2m, Incorporated has 3 FDA 510(k) cleared medical devices. Based in Leesburg, US.
Historical record: 3 cleared submissions from 2015 to 2016. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by K2m, Incorporated Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - K2m, Incorporated
3 devices