ARTHREX MENISCAL DART SYSTEM

ARTHREX MENISCAL DART SYSTEM is an FDA 510(k)-cleared medical device (K983577) manufactured by Arthrex, 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 12, 1999. Regulation: 8.