meddevicedb.com FDA Device Reference

SURGIFORM ANATOMICAL MALAR

K983756 Class II Special
Decision Date
1998-11-20
Sponsor / Applicant
Surgical Technology Laboratories, Inc.

Technical Specification

510(k) Submission ID K983756
Product Code LZK
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.3550
Decision Date 1998-11-20
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SURGIFORM ANATOMICAL MALAR received FDA 510(k) clearance under submission number K983756, sponsored by Surgical Technology Laboratories, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1998-11-20.

Classification & Regulation

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