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ENROUTE Enflate Transcarotid RX Balloon Dilatation Catheter

K221414 Class II Traditional
Decision Date
2022-09-02
Sponsor / Applicant
Silk Road Medical, Inc.

Technical Specification

510(k) Submission ID K221414
Product Code LIT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2022-09-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENROUTE Enflate Transcarotid RX Balloon Dilatation Catheter received FDA 510(k) clearance under submission number K221414, sponsored by Silk Road Medical, 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 2022-09-02.

Classification & Regulation

This clearance is catalogued under FDA product code LIT and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.