CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY— 510(k) K041315

Substantially Equivalent

Accuray, Inc.

FDA 510(k) clearance K041315 for CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY, Substantially Equivalent on 2004-06-10. Applicant: Accuray, Inc..

Clearance details

Applicant: Accuray, Inc.
Product code: Code IYE
Advisory panel: Radiology
Date received: 2004-05-17
Decision date: 2004-06-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Sunnyvale, CA, US

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Adverse events under product code IYE

product code IYE

Malfunction: 455
Other: 3
Total: 458

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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