510(k) K213645

Device
ClearPoint Maestro Brain Model
Applicant
ClearPoint Neuro, Inc.
510(k) number
K213645
Product code
QIH
Decision
Substantially Equivalent (SESE)
Decision date
2022-08-08
Date received
2021-11-18
Regulation
892.2050
Classification name
Automated Radiological Image Processing Software
Medical specialty
Radiology
Review panel
Radiology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Pete Piferi
Address
5 Musick Irvine CA US 92618 92618

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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