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Thompson Mis, Inc.
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BONEBAC T-PLIF INTERVERTEBRAL BODY FUSION DEVICE SYSTEM is an FDA 510(k)-cleared medical device (K111512) manufactured by Thompson Mis, 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 October 25, 2011. Regulation: 8.