Medical Device Manufacturer · US , Leesburg , VA

K2m, Incorporated - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2015

Total

Cleared

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

1-3 of 3