TENDON ROD MODEL OR41PO3-6

TENDON ROD MODEL OR41PO3-6 is an FDA 510(k)-cleared medical device (K781943) manufactured by Holter-Hausner Intl.. 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 3, 1978. Regulation: 8.