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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: K102380
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Product Description
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FDA Recall
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EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEM... 2 12/18/2024 MicroPort Orthopedics Inc.
EVOLUTION® MP Femoral CS/CR Non-Porous Non-porous MicroPort total knee replacement implants are f... 2 07/01/2024 MicroPort Orthopedics Inc.
EVOLUTION MP Tibial Bases, Size 2+ LEFT, REF ETPKN2PL, knee tibial base 2 11/22/2022 MicroPort Orthopedics Inc.
EVOLUTION MP Tibial Bases, Size 7 LEFT, REF ETPKN7SL, knee tibial base 2 11/22/2022 MicroPort Orthopedics Inc.
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