Medical Device Recalls
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1 result found
510(K) Number: K092308 |
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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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PoleStar system (N20 / N30) Warning Lamps Control Box, Warning Lamps Control Box Cables, Thermoflex ... | 2 | 07/06/2016 | Medtronic Navigation |
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