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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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 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 7 LEFT, REF ETPKN7SL, knee tibial base | 2 | 11/22/2022 | MicroPort Orthopedics Inc. |
| EVOLUTION MP Tibial Bases, Size 2+ LEFT, REF ETPKN2PL, knee tibial base | 2 | 11/22/2022 | MicroPort Orthopedics Inc. |
| EVOLUTION MP FEMORAL COMPONENT CS/CR POROUS SIZE 5 RIGHT PRIMARY, REF: EFSRP5PR; EVOLUTION MP FEM... | 2 | 12/18/2024 | MicroPort Orthopedics Inc. |
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