Medical Device Recalls
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1 result found
510(K) Number: K033972 |
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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 Orthopaedics Patella Assembly Instrument, REF 3182-1000, Non-Sterile, NDC (01) 0761332721585... | 2 | 09/13/2016 | Stryker Howmedica Osteonics Corp. |
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