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Muscle Stimulation System 110

K150742 Class II Special
Decision Date
2015-07-23
Sponsor / Applicant
Niveus Medical, Inc.

Technical Specification

510(k) Submission ID K150742
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2015-07-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Muscle Stimulation System 110 received FDA 510(k) clearance under submission number K150742, sponsored by Niveus Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2015-07-23.

Classification & Regulation

This clearance is catalogued under FDA product code IPF and 21 CFR 890.5850, within the Physical Medicine review panel as a Class II device.