LOGYK ACETABULAR COMPONENT SYSTEM

LOGYK ACETABULAR COMPONENT SYSTEM is an FDA 510(k)-cleared medical device (K931107) manufactured by Arthronics, 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 March 27, 1994. Regulation: 8.