ALTA FEMORAL INTRAMEDULLARY RODS/CFX RODS MODIFICATION

ALTA FEMORAL INTRAMEDULLARY RODS/CFX RODS MODIFICATION is an FDA 510(k)-cleared medical device (K935295) manufactured by Howmedica Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 10, 1994. Regulation: 8.