
Biopro, Inc.
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BIOPRO GLENOID COMPONENT W/ KEEL & W/ POSTS is an FDA 510(k)-cleared medical device (K001046) manufactured by Biopro, 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 June 7, 2000. Regulation: 8.