Medical Device Recalls
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1 result found
510(K) Number: K012702 |
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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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Endotec, Prosthesis Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer, Ti... | 2 | 05/20/2010 | Endotec, Inc. |
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