Medical Device Recalls
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1 result found
510(K) Number: K203005 |
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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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| MAZOR X robotic guidance system, Model TPL0059, with software versions 4.2.2 or 5.0.1 | 2 | 10/12/2023 |
FEI # 3005075696 Mazor Robotics Ltd |
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