ONEPORT SURGICAL TROCAR SYSTEM

ONEPORT SURGICAL TROCAR SYSTEM is an FDA 510(k)-cleared medical device (K073009) manufactured by Conmed Corporation. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 6, 2007. Regulation: 8.