Medical Device Recalls
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1 result found
510(K) Number: K190672 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software... | 1 | 12/22/2021 |
FEI # 1000517638 Medtronic Navigation, Inc. |
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