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V-Grip Detachment Controller for use with Hydrocoil Embolic System and MicroPlex Coil System, AZUR Detachment Controller for use with AZUR Peripheral Coil System

K162999 Class II Traditional
Decision Date
2017-03-29
Sponsor / Applicant
MicroVention, Inc.

Technical Specification

510(k) Submission ID K162999
Product Code HCG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5950
Decision Date 2017-03-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

V-Grip Detachment Controller for use with Hydrocoil Embolic System and MicroPlex Coil System, AZUR Detachment Controller for use with AZUR Peripheral Coil System received FDA 510(k) clearance under submission number K162999, sponsored by MicroVention, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2017-03-29.

Classification & Regulation

This clearance is catalogued under FDA product code HCG and 21 CFR 882.5950, within the Neurology review panel as a Class II device.