
Alliance Medical, Inc.
Free shipping on orders over $99 · 30-day returns
REPROCESSED LINVATEC ARTHROSCOPIC BURS is an FDA 510(k)-cleared medical device (K012630) manufactured by Alliance Medical, 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 November 8, 2001. Regulation: 8.