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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K083772
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FDA Recall
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Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7 2 12/13/2013 Aesculap, Inc.
Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Product Usage - The Colum... 2 06/26/2015 Aesculap Implant Systems
Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revision Knee Syst... 2 03/03/2016 Aesculap, Inc.
COLUMBUS REV F TIBIA OFFSET CEMENTED, Knee implant components, various sizes, model nos. NR068K NR... 2 03/13/2020 Aesculap Implant Systems LLC