DeviceClearance

THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/ RADIOTHERAPY V2.1— 510(k) K000478

Substantially Equivalent

Accuray, Inc.

FDA 510(k) clearance K000478 for THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/ RADIOTHERAPY V2.1, Substantially Equivalent on 2000-04-19. Applicant: Accuray, Inc..

Clearance details

Applicant
Accuray, Inc.
Product code
Code IWB
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Sunnyvale, CA, US
Download summary PDFView on FDA.gov ↗

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