PIXI YOUNG ADULT REFERENC POPULATION FOR OS CALCIS AND FOREARM

PIXI YOUNG ADULT REFERENC POPULATION FOR OS CALCIS AND FOREARM is an FDA 510(k)-cleared medical device (K972053) manufactured by Lunar Corp.. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 7, 1997. Regulation: 8.