ORTHOFIX TITANIUM HUMERAL PLATING SYSTEM LSP

ORTHOFIX TITANIUM HUMERAL PLATING SYSTEM LSP is an FDA 510(k)-cleared medical device (K062920) manufactured by Orthofix Srl. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on November 12, 2006. Regulation: 8.