Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K230064 |
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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 REF: TPL0059 | 2 | 01/16/2026 | Mazor Robotics Ltd |
| Mazor X. Model Number REF TPL0059; stereotaxic orthopedic instrument | 2 | 09/16/2024 | Mazor Robotics Ltd |
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