Stealthstation System Three Dimensional C-Arm Interface

FDA 510(k) K022414 · Medtronic Surgical Navigation Technologies

Substantially Equivalent

510(k) numberK022414

Submission

Device name
Stealthstation System Three Dimensional C-Arm Interface
Applicant
Medtronic Surgical Navigation Technologies
Louisville, CO, US
Received
July 24, 2002
Decision date
August 14, 2002
Decision
Substantially Equivalent (SESE)
Type
Special 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

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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
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
K003201Stealthstation Treatment Guidance PlatformHAW · Traditional 12/12/2000SE

Questions and answers

When was Stealthstation System Three Dimensional C-Arm Interface cleared by the FDA?

Stealthstation System Three Dimensional C-Arm Interface (K022414) received a 510(k) decision of Substantially Equivalent on August 14, 2002, 21 days after the submission was received.

What is the product code of K022414?

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