meddevicedb.com FDA Device Reference

Proton Positioing and Immobilization Devices

K180021 Class II Traditional
Decision Date
2018-06-29
Sponsor / Applicant
Medtec Inc Dba Civco Medical Solutions and Civco Radiotherap

Technical Specification

510(k) Submission ID K180021
Product Code IYE
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2018-06-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Proton Positioing and Immobilization Devices received FDA 510(k) clearance under submission number K180021, sponsored by Medtec Inc Dba Civco Medical Solutions and Civco Radiotherap. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2018-06-29.

Classification & Regulation

This clearance is catalogued under FDA product code IYE and 21 CFR 892.5050, within the Radiology review panel as a Class II device.