LINK SHOULDER PROSTHESIS ENDO-MODEL SYSTEM

LINK SHOULDER PROSTHESIS ENDO-MODEL SYSTEM is an FDA 510(k)-cleared medical device (K852365) 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 December 15, 1985. Regulation: 8.