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SPECTRUM DESIGNS SYMMETRICAL CHIN IMPLANT

K980138 Class II Traditional
Decision Date
1998-04-03
Sponsor / Applicant
Spectrum Designs, Inc.

Technical Specification

510(k) Submission ID K980138
Product Code FWP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3550
Decision Date 1998-04-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPECTRUM DESIGNS SYMMETRICAL CHIN IMPLANT received FDA 510(k) clearance under submission number K980138, sponsored by Spectrum Designs, 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 1998-04-03.

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.