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NCompass Nitinol Stone Extractors

K173009 Class II Traditional
Decision Date
2017-11-07
Sponsor / Applicant
Cook Incorporated

Technical Specification

510(k) Submission ID K173009
Product Code LQR
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5010
Decision Date 2017-11-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

NCompass Nitinol Stone Extractors received FDA 510(k) clearance under submission number K173009, sponsored by Cook Incorporated. 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 2017-11-07.

Classification & Regulation

This clearance is catalogued under FDA product code LQR and 21 CFR 876.5010, within the Gastroenterology, Urology review panel as a Class II device.