Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K053514 |
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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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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. |
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