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THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY

Page Type
Cleared 510(K)
510(k) Number
K984563
510(k) Type
Traditional
Applicant
ACCURAY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1999
Days to Decision
203 days
Submission Type
Summary

THE CYBERKNIFE SYSTEM FOR STEREOTACTIC RADIOSURGERY/RADIOTHERAPY

Page Type
Cleared 510(K)
510(k) Number
K984563
510(k) Type
Traditional
Applicant
ACCURAY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/14/1999
Days to Decision
203 days
Submission Type
Summary