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3D Bolus Software Application, 3D Brachy Software Application, Patient-Matched 3D Printed Radiation Therapy Accessory

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213438
510(k) Type
Traditional
Applicant
Adaptiiv
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
1/19/2022
Days to Decision
89 days
Submission Type
Summary

3D Bolus Software Application, 3D Brachy Software Application, Patient-Matched 3D Printed Radiation Therapy Accessory

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213438
510(k) Type
Traditional
Applicant
Adaptiiv
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
1/19/2022
Days to Decision
89 days
Submission Type
Summary