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My3D® Personalized Pelvic Reconstruction

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212815
510(k) Type
Traditional
Applicant
Onkos Surgical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2022
Days to Decision
306 days
Submission Type
Summary

My3D® Personalized Pelvic Reconstruction

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212815
510(k) Type
Traditional
Applicant
Onkos Surgical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/6/2022
Days to Decision
306 days
Submission Type
Summary