meddevicedb.com FDA Device Reference

SmartDrive Wheelchair Power Assist

K151199 Class II Traditional
Decision Date
2015-07-30
Sponsor / Applicant
Max Mobility, LLC

Technical Specification

510(k) Submission ID K151199
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2015-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SmartDrive Wheelchair Power Assist received FDA 510(k) clearance under submission number K151199, sponsored by Max Mobility, LLC. 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 2015-07-30.

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.