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Magellan Robotic System

K151730 Class II Special
Decision Date
2015-07-23
Sponsor / Applicant
Hansen Medical, Inc.

Technical Specification

510(k) Submission ID K151730
Product Code DXX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1290
Decision Date 2015-07-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Magellan Robotic System received FDA 510(k) clearance under submission number K151730, sponsored by Hansen Medical, 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 2015-07-23.

Classification & Regulation

This clearance is catalogued under FDA product code DXX and 21 CFR 870.1290, within the Cardiovascular review panel as a Class II device.