meddevicedb.com FDA Device Reference

SCISSORS: THOREK, JORGENSEN, FINOCHIETTO

K891203 Class I Traditional
Decision Date
1989-04-06
Sponsor / Applicant
Zinnanti Surgical Instruments, Inc.

Technical Specification

510(k) Submission ID K891203
Product Code LRW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1989-04-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SCISSORS: THOREK, JORGENSEN, FINOCHIETTO received FDA 510(k) clearance under submission number K891203, sponsored by Zinnanti Surgical Instruments, 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 1989-04-06.

Classification & Regulation

This clearance is catalogued under FDA product code LRW and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.