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AZUR DETACTABLE 18, MODELS 45-480305, 45-480310, 45-480405, 44-480415

K090168 Class II Special
Decision Date
2009-03-12
Sponsor / Applicant
MicroVention, Inc.

Technical Specification

510(k) Submission ID K090168
Product Code HCG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5950
Decision Date 2009-03-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AZUR DETACTABLE 18, MODELS 45-480305, 45-480310, 45-480405, 44-480415 received FDA 510(k) clearance under submission number K090168, sponsored by MicroVention, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2009-03-12.

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.