Medical Device Recalls
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1 result found
510(K) Number: K153345 |
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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 Universal Acetabular Cup Positioner/Impactor, REF 2101-0200, Non-Sterile, Howme... | 2 | 10/07/2016 | Stryker Howmedica Osteonics Corp. |
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