Clearance Summary
My3D® Personalized Pelvic Reconstruction received FDA 510(k) clearance under submission number K212815, sponsored by Onkos Surgical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2022-07-06.
- Submission: K212815
- Applicant / Sponsor: Onkos Surgical
- Clearance pathway: Traditional
- Review panel: Orthopedic
- Device class: Class II
- Regulation citation: 21 CFR 888.3358
- Decision date: 2022-07-06
Classification & Regulation
This clearance is catalogued under FDA product code LPH and 21 CFR 888.3358, within the Orthopedic review panel as a Class II device.