Leksell Vantage Stereotactic System

FDA 510(k) K171123 · Elekta Instrument AB

Substantially Equivalent

510(k) numberK171123

Submission

Device name
Leksell Vantage Stereotactic System
Applicant
Elekta Instrument AB
Stockholm, SE
Received
April 17, 2017
Decision date
September 15, 2017
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

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K160440Leksell Gamma Knife IconIWB · Traditional 04/20/2016SE
K152558Leksell Stereotactic System, Injection/ Aspiration Needle KitHAW · Special 03/02/2016SE
K151159Leksell Gamma Knife PerfexionIWB · Traditional 10/29/2015SE
K151666Leksell GammaPlanMUJ · Traditional 09/03/2015SE
K151561Leksell Gamma Knife IconIWB · Traditional 08/04/2015SE
K133565Leksell Gamma Knife PerfexionIWB · Traditional 05/09/2014SE
K120811Leksell Gamma Knife PerfexionIWB · Traditional 05/24/2012SE

Questions and answers

When was Leksell Vantage Stereotactic System cleared by the FDA?

Leksell Vantage Stereotactic System (K171123) received a 510(k) decision of Substantially Equivalent on September 15, 2017, 151 days after the submission was received.

What is the product code of K171123?

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