Medical Device Recalls
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1 result found
510(K) Number: K213302 |
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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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exoplan version 3.1 Rijeka Software -A medical software, intended to support the pre-operative plann... | 2 | 09/25/2023 | Exocad GmbH |
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