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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K052917
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FDA Recall
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Eius Unicompartmental Knee System Stryker Howmedica Osteonics Corp. Howmedica International S. de ... 2 01/11/2012 Stryker Howmedica Osteonics Corp.
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