POLLUX OA/POLLUX 30A/POLLUX 70A

POLLUX OA/POLLUX 30A/POLLUX 70A is an FDA 510(k)-cleared medical device (K953484) manufactured by Pollux Endoscopy, 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 31, 1995. Regulation: 8.