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6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter

K232190 Class II Special
Decision Date
2023-08-22
Sponsor / Applicant
Medtronic Vascular

Technical Specification

510(k) Submission ID K232190
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2023-08-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter received FDA 510(k) clearance under submission number K232190, sponsored by Medtronic Vascular. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2023-08-22.

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.