meddevicedb.com FDA Device Reference

C2000 POWERED WHEELCHAIR

K101524 Class II Traditional
Decision Date
2010-09-29
Sponsor / Applicant
Otto Bock Healthcare LP

Technical Specification

510(k) Submission ID K101524
Product Code ITI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3860
Decision Date 2010-09-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

C2000 POWERED WHEELCHAIR received FDA 510(k) clearance under submission number K101524, sponsored by Otto Bock Healthcare LP. 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 2010-09-29.

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.