meddevicedb.com FDA Device Reference

BACK TRAC

K781647 Class I Traditional
Decision Date
1978-10-17
Sponsor / Applicant
Tech Engineering, Inc.

Technical Specification

510(k) Submission ID K781647
Product Code HST
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.5850
Decision Date 1978-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BACK TRAC received FDA 510(k) clearance under submission number K781647, sponsored by Tech Engineering, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1978-10-17.

Classification & Regulation

This clearance is catalogued under FDA product code HST and 21 CFR 888.5850, within the Orthopedic review panel as a Class I device.