Medical Device Recalls
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1 result found
510(K) Number: K040749 |
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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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Modular Replacement System (MRS) Cemented Stems, Sterile, Catalog Numbers: 6485-3-000, 6485-3-008, 6... | 2 | 04/17/2009 | Stryker Howmedica Osteonics Corp. |
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