Medical Device Recalls
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1 result found
510(K) Number: K120812 |
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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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Carousel MAS1025-01, part of the Brain Surgical Accessories Intra-operative Kit (KIT0295), accessory... | 2 | 12/14/2018 | Mazor Robotics Ltd |
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