510(k) K240877

Device
Monteris Medical NeuroBlate System
Applicant
Monteris Medical,
510(k) number
K240877
Product code
ONO
Decision
Substantially Equivalent (SESE)
Decision date
2024-06-04
Date received
2024-03-29
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
No

Related Records

Applicant Contact

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

FDA Registration Numbers

Source Documents

510(k) summary PDF

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