Medical Device Recalls
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1 result found
510(K) Number: K072806 |
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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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Tibial Array and Femoral Array. Model Number(s): 0150ARR00001 and 0150ARR00002. Manufactured by: ... | 2 | 02/11/2009 | Mako Surgical Corporation |
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