K2m, Incorporated is one of 18433 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
K2m, Incorporated - FDA 510(k) Cleared Devices
Recent clearances: EVEREST Spinal System, Caspian OCT/MESA Mini/DENALI Mini Spinal System, RANGE/DENALI/MESA Spinal System
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.
510(k) submissions have been managed by K2m as regulatory consultant.
FDA 510(k) Regulatory Record - K2m, Incorporated
3 devices