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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
510(K) Number: K160700
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ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthropl... 2 02/09/2022 DePuy Orthopaedics, Inc.
ATTUNE REVISION DISTAL FEMORAL AUGMENT SZ 6 4MM- Intended as a Component in total knee arthroplasty ... 2 02/09/2022 DePuy Orthopaedics, Inc.
ATTUNE REVISION CEMENTED STEM 16X80MM-intended for use in total knee arthroplasty Part Number: 151... 2 08/25/2021 DePuy Orthopaedics, Inc.
ATTUNE Revision CRS Femoral LT SZ 5 Cemented, Catalog No. 150440105, Femoral Revision Implant, Knee 2 04/30/2018 DePuy Orthopaedics, Inc.
ATTUNE Revision CRS Femoral RT SZ 5 Cemented, Catalog No. 150440205, Femoral Revision Implant, Knee 2 04/30/2018 DePuy Orthopaedics, Inc.
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