Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K160700 |
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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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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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