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SelectSite C304 Deflectable Catheter System (C304); C315 Delivery System (C315)

K250558 Class II Special
Decision Date
2025-03-27
Sponsor / Applicant
Medtronic, Inc.

Technical Specification

510(k) Submission ID K250558
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2025-03-27
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SelectSite C304 Deflectable Catheter System (C304); C315 Delivery System (C315) received FDA 510(k) clearance under submission number K250558, sponsored by Medtronic, 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 2025-03-27.

Classification & Regulation

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