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

Total Devices2
Categories1
Latest FDA decision2023-06-27
TypeNumberDevice NameCodeDateActions
510(k) K213046 AceConnex Pre-Sutured FasciaGAT2023-06-27 View
510(k) K170957 ReConnex Pre-Sutured TendonGAT2018-03-20 View