Medical Device Recalls
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1 result found
510(K) Number: K140423 |
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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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Conformis iTotal CR G2 Knee Replacement System Catalog/Model #: M57250600010 Intended for use as... | 2 | 12/11/2014 | ConforMIS, Inc. |
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