Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K091999 |
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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 Robotic Radiosurgery System with 4D Planning procedure option of MultiPlan Treatment Plan... | 2 | 02/23/2012 | Accuray Incorporated |
CyberKnife Robotic Radiosurgery System: Lung Optimized Treatment option. The CyberKnife treatment... | 2 | 01/11/2012 | Accuray Incorporated |
CyberKnife Robotic Radiosurgery System, medical charged-particle radiation therapy system, manufactu... | 2 | 12/16/2010 | Accuray Inc |
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