meddevicedb.com FDA Device Reference

BACK ON TRACK INVERSION THERAPY & EXER

K823236 Class I Traditional
Decision Date
1983-01-21
Sponsor / Applicant
Lossing Orthopedic, Inc.

Technical Specification

510(k) Submission ID K823236
Product Code ION
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.5370
Decision Date 1983-01-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BACK ON TRACK INVERSION THERAPY & EXER received FDA 510(k) clearance under submission number K823236, sponsored by Lossing Orthopedic, 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 1983-01-21.

Classification & Regulation

This clearance is catalogued under FDA product code ION and 21 CFR 890.5370, within the Physical Medicine review panel as a Class I device.