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Alexandria Research Technologies, LLC
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TGS UNICOMPARTMENTAL KNEE ARTHROPLASTY (TGS UKA) MODULAR TIBIA SYSTEM is an FDA 510(k)-cleared medical device (K101206) manufactured by Alexandria Research Technologies, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 22, 2010. Regulation: 8.