meddevicedb.com FDA Device Reference

OFFSET ALUMINUM CANE

K790561 Class I Traditional
Decision Date
1979-04-03
Sponsor / Applicant
Maddak, Inc.

Technical Specification

510(k) Submission ID K790561
Product Code IPS
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3075
Decision Date 1979-04-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OFFSET ALUMINUM CANE received FDA 510(k) clearance under submission number K790561, sponsored by Maddak, 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 1979-04-03.

Classification & Regulation

This clearance is catalogued under FDA product code IPS and 21 CFR 890.3075, within the Physical Medicine review panel as a Class I device.