Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K170788 |
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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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CyberKnife Treatment Delivery System, REF 0660000 The CyberKnife System may be labeled as CyberKn... | 2 | 01/27/2025 | Accuray Incorporated |
CyberKnife Treatment Delivery System - Product Usage: indicated for image-guided stereotactic radios... | 2 | 03/17/2021 | Accuray Incorporated |
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