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3-D ACCUSCAN FACIAL IMPLANTS

K913761 Class II Traditional
Decision Date
1991-10-17
Sponsor / Applicant
Implantech Associates, Inc.

Technical Specification

510(k) Submission ID K913761
Product Code FWP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3550
Decision Date 1991-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

3-D ACCUSCAN FACIAL IMPLANTS received FDA 510(k) clearance under submission number K913761, sponsored by Implantech Associates, 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 1991-10-17.

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.