510(k) K233292

Device
ISIS Headboxes, ISIS Neurostimulator, ISIS Xpert Plus, ISIS Xpert, ISIS Xpress
Applicant
Inomed Medizintechnik GmbH
510(k) number
K233292
Product code
GWF
Decision
Substantially Equivalent (SESE)
Decision date
2023-10-27
Date received
2023-09-29
Regulation
882.1870
Classification name
Stimulator, Electrical, Evoked Response
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Tomasz Moszkowski
Address
Im Hausgruen 29 Emmendingen DE 79312 79312

FDA Registration Numbers

Source Documents

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

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