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ORTHOTIC BRACING

K761312 Class I Traditional
Decision Date
1977-01-10
Sponsor / Applicant
Hosmer Dorrance Corp.

Technical Specification

510(k) Submission ID K761312
Product Code IQI
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3475
Decision Date 1977-01-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHOTIC BRACING received FDA 510(k) clearance under submission number K761312, sponsored by Hosmer Dorrance Corp.. 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 1977-01-10.

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.