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MEDTRONIC ARES ANTIBIOTIC-IMPREGNATED CATHETER

K110560 Class II Traditional
Decision Date
2011-11-18
Sponsor / Applicant
Medtronic Neurosurgery

Technical Specification

510(k) Submission ID K110560
Product Code JXG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5550
Decision Date 2011-11-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDTRONIC ARES ANTIBIOTIC-IMPREGNATED CATHETER received FDA 510(k) clearance under submission number K110560, sponsored by Medtronic Neurosurgery. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2011-11-18.

Classification & Regulation

This clearance is catalogued under FDA product code JXG and 21 CFR 882.5550, within the Neurology review panel as a Class II device.