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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: K191779
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Product Description
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FDA Recall
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Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM, Part Number 151760118 2 03/17/2023 FEI # 1818910
DePuy Orthopaedics, Inc.
Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM, Part Number 151760312 2 03/17/2023 FEI # 1818910
DePuy Orthopaedics, Inc.
Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM, Part Number 151760226 2 03/17/2023 FEI # 1818910
DePuy Orthopaedics, Inc.
Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM, Part Number 151760212 2 03/17/2023 FEI # 1818910
DePuy Orthopaedics, Inc.
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