Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K953977 |
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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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Hip Prosthesis as a component of Primaloc Cementless/Collared Hip System. | 2 | 02/25/2003 | Ortho Development Corporation |
Hip Prosthesis as a component of Primaloc Cementless/Collarless Hip System | 2 | 02/25/2003 | Ortho Development Corporation |
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