Medical Device Recalls
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1 result found
510(K) Number: K955731 |
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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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Solar Shoulder Humeral Stem These devices are modular components of a total shoulder system. Thes... | 2 | 01/26/2009 | Stryker Howmedica Osteonics Corp. |
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