MEGA PLUS SUPER LAG SCREW

MEGA PLUS SUPER LAG SCREW is an FDA 510(k)-cleared medical device (K930156) manufactured by Pfizer Hospital Products Group, 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 February 21, 1994. Regulation: 8.