Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K083772 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Aesculap Columbus Revision CoCr 15mm distal and posterior spacers, sizes F5-F7 | 2 | 12/13/2013 | 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 |
Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revision Knee Syst... | 2 | 03/03/2016 | Aesculap, Inc. |
Columbus Tibia Plateau (component of the Columbus REVISION Knee System) Product Usage - The Colum... | 2 | 06/26/2015 | Aesculap Implant Systems |
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