Stealthstation Treatment Guidance Platform

FDA 510(k) K003201 · Medtronic Surgical Navigation Technologies

Substantially Equivalent

510(k) numberK003201

Submission

Device name
Stealthstation Treatment Guidance Platform
Applicant
Medtronic Surgical Navigation Technologies
Louisville, CO, US
Received
October 12, 2000
Decision date
December 12, 2000
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HAW – Neurological Stereotaxic Instrument
Device class
Class II (moderate risk)
Regulation
21 CFR 882.4560
Specialty
Neurology

Other 510(k)s with product code HAW

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K253856Geniant Cranial (Navigated Neurosurgical Positioning Robot)HAW · Traditional Koh Young Technology, Inc.09/10/2026SE
K261932Leksell® Vantage Stereotactic SystemHAW · Traditional Elekta Solutions AB08/05/2026SE
K253663Zeta Navigation SystemHAW · Traditional Zeta Surgical, Inc.05/01/2026SE
K253379Stealth AXiS Cranial clinical applicationHAW · Traditional Medtronic Navigation, Inc.03/26/2026SE
K231897NeuroAlign softwareHAW · Traditional Medivis, Inc.10/21/2025SE
K251317SOLOPASS 2.0 SystemHAW · Traditional Intravent Medical Partners09/05/2025SE
K250893Ball Joint Guide Array (66295)HAW · Traditional Bayer Medical Care, Inc.09/04/2025SE
K250505Ez-FiducialsHAW · Traditional Phasor Health, LLC07/09/2025SE
K242575Stereotaxic Guiding Surgical Devices, NaoTrac SHAW · Traditional Brain Navi Biotechnology Co., Ltd.05/23/2025SE
K241327Navient Image Guide Navigation System (955-NC-NC), CranialHAW · Traditional Claronav02/05/2025SE

More from Claronav

510(k)DeviceDecision
K050438Stealthstation System UpdateHAW · Special 06/02/2005SE
K043088Medtronic SNT Stealthstation Axiem Imageless Knee ModuleHAW · Traditional 01/05/2005SE
K030552Imageless Knee Module for the Stealthstation SystemHAW · Special 03/19/2003SE
K030106Stealthstation System Advanced Contour Registration Software ModuleHAW · Special 02/12/2003SE
K022126Catheter Introducer for the Stealthstation SystemHAW · Traditional 01/03/2003SE
K021980Hip Module for the Stealthstation SystemHAW · Traditional 11/19/2002SE
K022414Stealthstation System Three Dimensional C-Arm InterfaceHAW · Special 08/14/2002SE
K020338Stealthstation with Fluoromerge SoftwareHAW · Special 02/27/2002SE
K012937Knee Module for the Stealthstation SystemHAW · Traditional 01/25/2002SE
K002869Localisa Cardiac Navigation SystemDQK · Traditional 03/27/2001SE

Questions and answers

When was Stealthstation Treatment Guidance Platform cleared by the FDA?

Stealthstation Treatment Guidance Platform (K003201) received a 510(k) decision of Substantially Equivalent on December 12, 2000, 61 days after the submission was received.

What is the product code of K003201?

The FDA product code is HAW – Neurological Stereotaxic Instrument, a Class II (moderate risk) device regulated under 21 CFR 882.4560.