Medical Device Recalls
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1 result found
510(K) Number: K122883 |
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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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EXp Tibial Insert ; Intended Use of Device(s): The Proven Gen-Flex Total Knee System is intended fo... | 2 | 01/14/2015 | Stelkast Co |
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