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HUMERAL FRACTURE CAST BRACE

K811343 Class I Traditional
Decision Date
1981-05-28
Sponsor / Applicant
Deseret Medical, Inc.

Technical Specification

510(k) Submission ID K811343
Product Code IQI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3475
Decision Date 1981-05-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HUMERAL FRACTURE CAST BRACE received FDA 510(k) clearance under submission number K811343, sponsored by Deseret Medical, 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 1981-05-28.

Classification & Regulation

This clearance is catalogued under FDA product code IQI and 21 CFR 890.3475, within the Physical Medicine review panel as a Class I device.