meddevicedb.com FDA Device Reference

Frontier Series Power Wheelchairs

K213090 Class II Traditional
Decision Date
2021-11-19
Sponsor / Applicant
Magic Mobility

Technical Specification

510(k) Submission ID K213090
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2021-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Frontier Series Power Wheelchairs received FDA 510(k) clearance under submission number K213090, sponsored by Magic Mobility. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2021-11-19.

Classification & Regulation

This clearance is catalogued under FDA product code ITI and 21 CFR 890.3860, within the Physical Medicine review panel as a Class II device.