PROFEMUR HIP SYSTEM MODULAR NECKS

PROFEMUR HIP SYSTEM MODULAR NECKS is an FDA 510(k)-cleared medical device (K100866) manufactured by Wrightmedicaltechnologyinc. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 27, 2010. Regulation: 8.