Medical Device Recalls
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1 result found
510(K) Number: K101939 |
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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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OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails | 2 | 11/06/2020 | Merete Medical GmbH |
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