meddevicedb.com FDA Device Reference

START JUNIOR

K073512 Class I Traditional
Decision Date
2008-01-14
Sponsor / Applicant
Otto Bock Healthcare LP

Technical Specification

510(k) Submission ID K073512
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2008-01-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

START JUNIOR received FDA 510(k) clearance under submission number K073512, 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 2008-01-14.

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.