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STRAITH CHIN IMPLANTS

K801073 Class II Traditional
Decision Date
1980-05-20
Sponsor / Applicant
Surgical Technology Laboratories, Inc.

Technical Specification

510(k) Submission ID K801073
Product Code FWP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3550
Decision Date 1980-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STRAITH CHIN IMPLANTS received FDA 510(k) clearance under submission number K801073, sponsored by Surgical Technology Laboratories, 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 1980-05-20.

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.