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HIP ABDUCTION SPLINT

K810557 Class I Traditional
Decision Date
1981-03-13
Sponsor / Applicant
Orthomedics

Technical Specification

510(k) Submission ID K810557
Product Code IOZ
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3665
Decision Date 1981-03-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HIP ABDUCTION SPLINT received FDA 510(k) clearance under submission number K810557, sponsored by Orthomedics. 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 1981-03-13.

Classification & Regulation

This clearance is catalogued under FDA product code IOZ and 21 CFR 890.3665, within the Physical Medicine review panel as a Class I device.