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VitalStim(R) Plus Electrotherapy System

K153224 Class II Traditional
Decision Date
2016-02-17
Sponsor / Applicant
Djo, LLC

Technical Specification

510(k) Submission ID K153224
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 2016-02-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VitalStim(R) Plus Electrotherapy System received FDA 510(k) clearance under submission number K153224, sponsored by Djo, 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 2016-02-17.

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.