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EXCELSIOR XT-27 MICROCATHETER

K113778 Class II Traditional
Decision Date
2012-04-20
Sponsor / Applicant
Stryker Neurovascular

Technical Specification

510(k) Submission ID K113778
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2012-04-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EXCELSIOR XT-27 MICROCATHETER received FDA 510(k) clearance under submission number K113778, sponsored by Stryker Neurovascular. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-04-20.

Classification & Regulation

This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.