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MODIFICATION TO:CONTOUR SE MICROSPHERES

K071634 Class II Special
Decision Date
2007-07-12
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K071634
Product Code HCG
Medical Specialty / Panel Neurology
Regulation Citation 21 CFR 882.5950
Decision Date 2007-07-12
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO:CONTOUR SE MICROSPHERES received FDA 510(k) clearance under submission number K071634, sponsored by Boston Scientific Corp. The device was reviewed via the Special premarket notification pathway and assigned to the Neurology review panel. The statutory decision date of record is 2007-07-12.

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.