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HOFFMAN UNIVERSAL FOOT SUPPORT

K821252 Class I Traditional
Decision Date
1982-06-22
Sponsor / Applicant
Howmedica Corp.

Technical Specification

510(k) Submission ID K821252
Product Code KQZ
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.5890
Decision Date 1982-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOFFMAN UNIVERSAL FOOT SUPPORT received FDA 510(k) clearance under submission number K821252, sponsored by Howmedica Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1982-06-22.

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.