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U.S. Department of Health and Human Services

Medical Device Recalls

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510(K) Number: K040734
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Product Description
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FDA Recall
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Stryker Orthopaedics Restoration Modular Cone Body Trials Stryker Ireland Carrigtwohill Industrial ... 2 09/28/2012 Stryker Howmedica Osteonics Corp.
Restoration Modular Cone Bodies; titanium Alloy and Hydroxyapatite, Sterile. Catalog number 6276-1-... 2 05/21/2009 Stryker Howmedica Osteonics Corp.