Medical Device Recalls
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1 result found
510(K) Number: K090988 |
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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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The GMK knee system: designed for cemented use in total knee arthroplasty. Sphere and Primary Inser... | 2 | 12/20/2017 | Medacta Usa Inc |
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