meddevicedb.com FDA Device Reference

BACKTRAC 90-90 TRACTION

K802869 Class I Traditional
Decision Date
1980-12-11
Sponsor / Applicant
Backtrac

Technical Specification

510(k) Submission ID K802869
Product Code KQZ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.5890
Decision Date 1980-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BACKTRAC 90-90 TRACTION received FDA 510(k) clearance under submission number K802869, sponsored by Backtrac. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1980-12-11.

Classification & Regulation

This clearance is catalogued under FDA product code KQZ and 21 CFR 888.5890, within the Orthopedic review panel as a Class I device.