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MILLENIUM II

K081665 Class I Traditional
Decision Date
2008-06-27
Sponsor / Applicant
Next Mobility, LLC

Technical Specification

510(k) Submission ID K081665
Product Code IOR
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3850
Decision Date 2008-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MILLENIUM II received FDA 510(k) clearance under submission number K081665, sponsored by Next 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 2008-06-27.

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.