ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM

ELLIPSE PRECICE INTRAMEDULLARY LIMB LENGTHENING SYSTEM is an FDA 510(k)-cleared medical device (K131490) manufactured by Ellipse Technologies, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 22, 2014. Regulation: 8.