meddevicedb.com FDA Device Reference

EXTENTRAC ELITE

K031996 Class II Abbreviated
Decision Date
2004-07-23
Sponsor / Applicant
Advanced Back Technologies

Technical Specification

510(k) Submission ID K031996
Product Code ITH
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5900
Decision Date 2004-07-23
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXTENTRAC ELITE received FDA 510(k) clearance under submission number K031996, sponsored by Advanced Back Technologies. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 2004-07-23.

Classification & Regulation

This clearance is catalogued under FDA product code ITH and 21 CFR 890.5900, within the Physical Medicine review panel as a Class II device.