ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002

ARTHROSCOPIC SURGICAL KNIVES MODELS 1001 AND 1002 is an FDA 510(k)-cleared medical device (K903213) manufactured by Percutaneous Technologies. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 26, 1990. Regulation: 8.