Medical Device Recalls
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1 result found
510(K) Number: K153326 |
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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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Erisma- LP posterior fixation system with the below specifically affected products: 1. Erisma-L... | 3 | 07/18/2019 | Clariance Inc |
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