meddevicedb.com FDA Device Reference

Mimics Thoracic Planner

K251964 Class II Traditional
Decision Date
2026-03-12
Sponsor / Applicant
Materialise NV

Technical Specification

510(k) Submission ID K251964
Product Code LLZ
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.2050
Decision Date 2026-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Mimics Thoracic Planner received FDA 510(k) clearance under submission number K251964, sponsored by Materialise NV. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2026-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code LLZ and 21 CFR 892.2050, within the Radiology review panel as a Class II device.