Medical Device Recalls
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1 result found
510(K) Number: K062113 |
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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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ReUnion Fracture Stem Humeral Component - PureFix HA; Shoulder prosthesis. Distal Diameter - 7 to... | 2 | 11/01/2007 | Stryker Howmedica Osteonics Corp. |
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