CYPRESS CANNULATED BONE SCREW

CYPRESS CANNULATED BONE SCREW is an FDA 510(k)-cleared medical device (K894830) manufactured by Cypress Medical Mfg., 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 August 29, 1989. Regulation: 8.