CO2 ARTHROFLATOR

CO2 ARTHROFLATOR is an FDA 510(k)-cleared medical device (K953550) manufactured by KARL STORZ Endoscopy-America, 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 22, 1995. Regulation: 8.