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U.S. Department of Health and Human Services

510(k) Premarket Notification
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Device Classification Name Accelerator, Linear, Medical
510(k) Number K072504
Device Name CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM
Applicant
Accuray Incorporated
1310 Chesapeake Terrace
Sunnyvale,  CA  94089
Applicant Contact ANNE SCHLAGENHAFT
Correspondent
Accuray Incorporated
1310 Chesapeake Terrace
Sunnyvale,  CA  94089
Correspondent Contact ANNE SCHLAGENHAFT
Regulation Number892.5050
Classification Product Code
IYE  
Date Received09/06/2007
Decision Date 09/21/2007
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Radiology
510k Review Panel Radiology
Summary Summary
Type Special
Reviewed by Third Party No
Combination Product No
Predetermined Change
Control Plan Authorized		 No
Recalls CDRH Recalls
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