DeviceClearance

CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY— 510(k) K052325

Substantially Equivalent

Accuray Incorporated

FDA 510(k) clearance K052325 for CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY, Substantially Equivalent on 2005-09-14. Applicant: Accuray Incorporated.

Clearance details

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.