Medical Device Recalls
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1 result found
510(K) Number: K102019 |
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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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Stryker Howmedica Osteonics RESTORATION Acetabular Augment System; Howmedica Osteonics Corp., A sub... | 2 | 05/19/2015 | Stryker Howmedica Osteonics Corp. |
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