meddevicedb.com FDA Device Reference

VitalFlow Set with Balance™ Biosurface

K261335 Class II Traditional
Decision Date
2026-07-31
Sponsor / Applicant
Medtronic, Inc.

Technical Specification

510(k) Submission ID K261335
Product Code QJZ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4100
Decision Date 2026-07-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VitalFlow Set with Balance™ Biosurface received FDA 510(k) clearance under submission number K261335, sponsored by Medtronic, 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 2026-07-31.

Classification & Regulation

This clearance is catalogued under FDA product code QJZ and 21 CFR 870.4100, within the Cardiovascular review panel as a Class II device.