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S-250 PROTON BEAM RADIATION THERAPY SYSTEM

K120676 Class II Traditional
Decision Date
2012-06-04
Sponsor / Applicant
Mevion Medical Systems

Technical Specification

510(k) Submission ID K120676
Product Code LHN
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5050
Decision Date 2012-06-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

S-250 PROTON BEAM RADIATION THERAPY SYSTEM received FDA 510(k) clearance under submission number K120676, sponsored by Mevion Medical Systems. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2012-06-04.

Classification & Regulation

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