meddevicedb.com FDA Device Reference

Merit Siege Vascular Plug

K212817 Class II Traditional
Decision Date
2021-12-15
Sponsor / Applicant
Merit Medical System, Inc.

Technical Specification

510(k) Submission ID K212817
Product Code KRD
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3300
Decision Date 2021-12-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Merit Siege Vascular Plug received FDA 510(k) clearance under submission number K212817, sponsored by Merit Medical System, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2021-12-15.

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.