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MEDTRONIC CLIP GUN KIT

K050044 Class II Special
Decision Date
2005-02-07
Sponsor / Applicant
Medtronic Neurosurgery

Technical Specification

510(k) Submission ID K050044
Product Code HBO
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.4150
Decision Date 2005-02-07
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDTRONIC CLIP GUN KIT received FDA 510(k) clearance under submission number K050044, sponsored by Medtronic Neurosurgery. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2005-02-07.

Classification & Regulation

This clearance is catalogued under FDA product code HBO and 21 CFR 882.4150, within the Neurology review panel as a Class II device.