Arthrex Vortex Threaded Bone Marrow Recovery Needle

Arthrex Vortex Threaded Bone Marrow Recovery Needle is an FDA 510(k)-cleared medical device (K213213) manufactured by Arthrex, Inc.. 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 November 18, 2021. Regulation: 8.