INTER-OS LIMB LENGTHENER

INTER-OS LIMB LENGTHENER is an FDA 510(k)-cleared medical device (K031875) manufactured by Inter-Os Technologies. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 21, 2003. Regulation: 8.