meddevicedb.com FDA Device Reference

DURALASTIC ANATOMICAL CHIN IMPLANTS

K971478 Class II Traditional
Decision Date
1997-07-18
Sponsor / Applicant
Allied Biomedical Corp.

Technical Specification

510(k) Submission ID K971478
Product Code FWP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3550
Decision Date 1997-07-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DURALASTIC ANATOMICAL CHIN IMPLANTS received FDA 510(k) clearance under submission number K971478, sponsored by Allied Biomedical Corp.. 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 1997-07-18.

Classification & Regulation

This clearance is catalogued under FDA product code FWP and 21 CFR 878.3550, within the General, Plastic Surgery review panel as a Class II device.