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NEUROTECH-4 PROGRAM NEUROMUSCULAR STIMULATOR 281

K860314 Class II Traditional
Decision Date
1986-06-17
Sponsor / Applicant
Neurotech, Inc.

Technical Specification

510(k) Submission ID K860314
Product Code IPF
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5850
Decision Date 1986-06-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NEUROTECH-4 PROGRAM NEUROMUSCULAR STIMULATOR 281 received FDA 510(k) clearance under submission number K860314, sponsored by Neurotech, Inc.. 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 1986-06-17.

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.