Medical Device Recalls
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1 result found
510(K) Number: K103010 |
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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 CMF Customized Implant Kit X-Large; 5444-0-401 X-Large Implant (2) 5444-01-102 Host Bone; ... | 2 | 02/12/2014 | Stryker Howmedica Osteonics Corp. |
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