Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K162309 |
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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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Stealth S8 Clinical Software Application, REF: 9735762, CE0344, Rx Only. Used in the StealthStation... | 1 | 05/09/2024 | Medtronic Navigation, Inc. |
Medtronic Nexframe Stereotactic System and StealthStation Cranial software version 3.0 or newer with... | 1 | 05/18/2020 | Medtronic Navigation, Inc. |
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