Last synced on 14 November 2025 at 11:06 pm

My3D® Personalized Pelvic Reconstruction

Page Type
Cleared 510(K)
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)
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