LUHR TITANIUM PAN FIXATION SYSTEM

LUHR TITANIUM PAN FIXATION SYSTEM is an FDA 510(k)-cleared medical device (K945139) manufactured by Howmedica Corp.. 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 11, 1995. Regulation: 8.