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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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51 records meeting your search criteria returned- Product Code: KRO Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
AESCULAP AG AS ENDURO FEM.SPACER POST/DIST F2 4X8MM 04/10/2019
AESCULAP AG AS NUT F/FEMUR EXTENS.STEM ALL SZ.NEUTR. 04/10/2019
AESCULAP AG AS ENDURO FEM.SPACER POST/DIST F2 4X8MM 04/10/2019
AESCULAP AG AS TIBIA OFFSET STEM D12X92MM CEMENTED 04/10/2019
AESCULAP AG AS FEMUR EXTENS.STEM 6° D18X77 CEMENTED 04/10/2019
AESCULAP AG AS ENDURO TIBIA HEMI-WEDGE T1 4MM RM/LL 04/10/2019
AESCULAP AG AS ENDURO TIBIA HEMI-WEDGE T1 4MM RL/LM 04/10/2019
AESCULAP AG AS ENDURO FEMORAL COMPONENT CEMENTED F2L 04/10/2019
AESCULAP AG AS ENDURO TIBIAL COMP.OFFSET CEMENTED T1 04/10/2019
AESCULAP AG AS ENDURO MENISCAL COMPONENT F2 16MM 04/10/2019
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