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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 4 of 4 Results
510(K) Number: K122137
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FDA Recall
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CyberKnife Robotic Radiosurgery System using software version 10.6; Catalog/Part Number: 54000 UDI... 2 12/12/2016 Accuray Incorporated
CyberKnife Robotic Radiosurgery System with the first generation IRIS Variable Aperture Collimator. ... 2 11/14/2014 Accuray Incorporated
Accuray CyberKnife Robotic Radiosurgery System; Accuray Incorporated Sunnyvale, CA. Indicated for... 2 01/27/2014 Accuray Incorporated
Accuray CyberKnife System Medical Physicist, Robotic Radiosurgery System, Medical charged-particle r... 2 04/16/2013 Accuray Incorporated
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