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Alexandria Research Technologies, LLC

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K101206 TGS UNICOMPARTMENTAL KNEE ARTHROPLASTY (TGS UKA) MODULAR TIBIA SYSTEMHSX2010-07-23 View
510(k) K090024 TGS UNICOMPARTMENTAL KNEE ARTHROPLASTY SYSTEMHSX2009-05-04 View
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