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CHISELS- FREER, LUCAS, ALEXANDER, BISHOP

K891902 Class II Traditional
Decision Date
1989-04-12
Sponsor / Applicant
Zinnanti Surgical Instruments, Inc.

Technical Specification

510(k) Submission ID K891902
Product Code KGD
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1989-04-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHISELS- FREER, LUCAS, ALEXANDER, BISHOP received FDA 510(k) clearance under submission number K891902, sponsored by Zinnanti Surgical Instruments, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1989-04-12.

Classification & Regulation

This clearance is catalogued under FDA product code KGD and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.