Medical Device Recalls
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1 result found
510(K) Number: K110533 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
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Recalling Firm
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ShapeMatch Cutting Guides Product Usage: The ShapeMatch Cutting Guides are intended to be used a... | 1 | 04/12/2013 | Stryker Howmedica Osteonics Corp. |
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