LINK GIEBEL BLADE PLATE SYSTEM

LINK GIEBEL BLADE PLATE SYSTEM is an FDA 510(k)-cleared medical device (K895507) manufactured by Link America, 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 12, 1990. Regulation: 8.