510(k) K190047

StimRouter Neuromodulation System by Bioness, Inc. — Product Code GZF

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 31, 2019
Date Received
January 9, 2019
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stimulator, Peripheral Nerve, Implanted (Pain Relief)
Device Class
Class II
Regulation Number
882.5870
Review Panel
NE
Submission Type