Medical Device Recalls
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1 result found
510(K) Number: K153660 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Medtronic Nexframe Stereotactic System and StealthStation Cranial software version 3.0 or newer with... | 1 | 05/18/2020 |
FEI # 1000517638 Medtronic Navigation, Inc. |
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