APTUS ULNA SHORTENING 2.5

APTUS ULNA SHORTENING 2.5 is an FDA 510(k)-cleared medical device (K141232) manufactured by Medartis AG. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 22, 2014. Regulation: 8.