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SMALL BONE FIXATION SYSTEM

K911929 Class I Traditional
Decision Date
1991-07-02
Sponsor / Applicant
United American Medical Co., Inc.

Technical Specification

510(k) Submission ID K911929
Product Code HWE
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4820
Decision Date 1991-07-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMALL BONE FIXATION SYSTEM received FDA 510(k) clearance under submission number K911929, sponsored by United American Medical Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1991-07-02.

Classification & Regulation

This clearance is catalogued under FDA product code HWE and 21 CFR 878.4820, within the General, Plastic Surgery review panel as a Class I device.