SPONGER CABLE SYSTEM, MODIFICATION

SPONGER CABLE SYSTEM, MODIFICATION is an FDA 510(k)-cleared medical device (K935481) manufactured by Pioneer Surgical Technology. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 25, 1994. Regulation: 8.