510(k) K260976

Device
NeuroBlate System
Applicant
Monteris Medical
510(k) number
K260976
Product code
ONO
Decision
Substantially Equivalent (SESE)
Decision date
2026-04-23
Date received
2026-03-24
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
Special
Statement or summary
Summary
Third party reviewed
N

Applicant Contact#

Contact
David Mueller
Address
131 Cheshire Ln. Suite 100 Minnetonka MN US 55305 55305

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code ONO#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K253391Visualase Cooled Laser Applicator System (9735559); Visualase Cooled Laser Applicator System (9735560); Visualase Cooled Laser Applicator System (9735561)Medtronic Navigation, Inc.2026-03-13
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