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Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs

K181090 Class I Traditional
Decision Date
2018-11-14
Sponsor / Applicant
Invacare Corporation

Technical Specification

510(k) Submission ID K181090
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2018-11-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Invacare® Solara® 3G and Solara® 3G Spree Manual Wheelchairs received FDA 510(k) clearance under submission number K181090, sponsored by Invacare Corporation. 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 2018-11-14.

Classification & Regulation

This clearance is catalogued under FDA product code IOR and 21 CFR 890.3850, within the Physical Medicine review panel as a Class I device.