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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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17 records meeting your search criteria returned- Product Code: KRO Product Problem: Device Appears to Trigger Rejection Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
MEDACTA INTERNATIONAL SA GMK-HINGE FIXED TIBIAL INSERT SIZE 2/12M 11/08/2022
MEDACTA INTERNATIONAL SA GMK-HINGE 02.09.0414H FIXED TIBIAL INSER 10/31/2022
MEDACTA INTERNATIONAL SA GMK-HINGE FIXED TIBIAL INSERT SIZE 6/14M 10/14/2022
MEDACTA INTERNATIONAL SA GMK-HINGE FIXED TIBIAL INSERT SIZE 3/12M 08/30/2022
MEDACTA INTERNATIONAL SA GMK-HINGE 02.09.0412H FIXED TIBIAL INSER 08/26/2022
AESCULAP AG AS FEMUR EXTENS.STEM 6° D12X77 CEMENTED 05/20/2022
AESCULAP AG AS COLUMBUS REV FEM.SPACER POST.F5 5MM 05/20/2022
AESCULAP AG AS FEMUR EXTENS.STEM 6° D12X77 CEMENTED 05/20/2022
AESCULAP AG COLUMBUS REV F HC GLID.SURF.T1/1+ 12MM 05/20/2022
AESCULAP AG AS TIBIA OFFSET STEM D12X52MM CEMENTED 05/20/2022
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