FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

Cube 4D Navigation System, VirtuEye Pro

K Number: K261540 · Decision Jun 2, 2026
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
36
Applicant Total
16
Review Days
25

Basic Information

Device Name
Cube 4D Navigation System, VirtuEye Pro
K Number
K261540
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Fiagon GmbH
Date Received
May 8, 2026
Decision Date
June 2, 2026
Product Code
PGW
Advisory Committee
Neurology
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PGW Ear, Nose, And Throat Stereotaxic Instrument

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PGW), ordered by most recent decision date.

View all

Other Clearances by Fiagon GmbH

K Number Device Name
K230700 RIWOtrack Navigation System
K230065 VenSure™ Balloon Dilation System, VenSure™ Light Balloon Dilation System, VenSure™ Nav Balloon Dilation System, VenSure™ ET Balloon Dilation System
K211291 Cube Navigation System, VirtuEye V2, Navigation Sensor NanoRest, Navigation Unit Cube 4D
K201472 VenSure Balloon Device, VenSure Nav Balloon Device
K200041 FlexPointer 1.5 Single Use, FlexTube 3 Single Use
K163209 Fiagon Navigation System
K163416 Fiagon Navigation – PointerTube Straight and PointerTube Keat
K162176 Fiagon Navigation System
K161940 Guidewire 0.6 Single Use
K151156 Fiagon Navigation System
Search all 16 clearances from Fiagon GmbH →