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Instinct Plus Endoscopic Clipping Device

K212323 Class II Special
Decision Date
2021-08-25
Sponsor / Applicant
Wilson-Cook Medical, Inc.

Technical Specification

510(k) Submission ID K212323
Product Code PKL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4400
Decision Date 2021-08-25
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Instinct Plus Endoscopic Clipping Device received FDA 510(k) clearance under submission number K212323, sponsored by Wilson-Cook Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2021-08-25.

Classification & Regulation

This clearance is catalogued under FDA product code PKL and 21 CFR 876.4400, within the Gastroenterology, Urology review panel as a Class II device.