MODIFICATION TO CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM— 510(k) K091146

Substantially Equivalent

Accuray, Inc.

FDA 510(k) clearance K091146 for MODIFICATION TO CYBERKNIFE ROBOTIC RADIOSURGERY SYSTEM, Substantially Equivalent on 2009-05-01. Applicant: Accuray, Inc..

Clearance details

Applicant: Accuray, Inc.
Product code: Code MUJ
Advisory panel: Radiology
Date received: 2009-04-20
Decision date: 2009-05-01
Decision: Substantially Equivalent
Clearance type: Special
Location: Sunnyvale, CA, US

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