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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
510(K) Number: K053514
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Product Description
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FDA Recall
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Howmedica Osteonics Corp. Stryker Orthopaedics Specialty Triathlon Left and Right A//P Sizer Adjust... 2 03/18/2013 Stryker Howmedica Osteonics Corp.
Triathlon Cemented Stem - Knee These devices are modular components of a total knee system. These... 2 01/26/2009 Stryker Howmedica Osteonics Corp.