510(k) K253391

Device
Visualase Cooled Laser Applicator System (9735559); Visualase Cooled Laser Applicator System (9735560); Visualase Cooled Laser Applicator System (9735561)
Applicant
Medtronic Navigation, Inc.
510(k) number
K253391
Product code
ONO
Decision
Substantially Equivalent (SESE)
Decision date
2026-03-13
Date received
2025-09-30
Regulation
878.4810
Classification name
Neurosurgical Laser With Mr Thermography
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Sharon McDermott
Address
200 Medtronic Dr. Lafayette CO US 80026 80026

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

Other 510(k) Records For Product Code ONO

510(k)DeviceApplicantDecision date
K260976NeuroBlate SystemMonteris Medical2026-04-23
K251298Mobile Laser Unit (1001-N2); Thermoguide Workstation (1100-N1); Laser Applicator (4012-N5, 4017-N2, 4017-N4); MR Introducer (4013-N6)Clinical Laserthermia Systems, AB2025-09-04
K250307Visualase V2 MRI-guided Laser Ablation System (9736422)Medtronic Navigation2025-05-29
K240877Monteris Medical NeuroBlate SystemMonteris Medical,2024-06-04
K214125TRANBERG Thermoguide Therapy SystemClinical Laserthermia Systems, AB2022-09-22
K211269Visualase MRI-Guided Laser Ablation System (SW 3.4)Medtronic Navigation, Inc.2022-01-07