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Gel-Block 10X embolization pledgets

K143038 Class II Special
Decision Date
2014-11-20
Sponsor / Applicant
Vascular Solutions, Inc.

Technical Specification

510(k) Submission ID K143038
Product Code KRD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3300
Decision Date 2014-11-20
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Gel-Block 10X embolization pledgets received FDA 510(k) clearance under submission number K143038, sponsored by Vascular Solutions, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2014-11-20.

Classification & Regulation

This clearance is catalogued under FDA product code KRD and 21 CFR 870.3300, within the Cardiovascular review panel as a Class II device.