
Avitus Orthopaedics, Inc.
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Avitus(r) Bone Harvester is an FDA 510(k)-cleared medical device (K210631) manufactured by Avitus Orthopaedics, 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 March 30, 2021. Regulation: 8.