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StimRouter Neuromodulation System

Page Type
Cleared 510(K)
510(k) Number
K190047
510(k) Type
Traditional
Applicant
Bioness Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2019
Days to Decision
295 days
Submission Type
Summary

StimRouter Neuromodulation System

Page Type
Cleared 510(K)
510(k) Number
K190047
510(k) Type
Traditional
Applicant
Bioness Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/2019
Days to Decision
295 days
Submission Type
Summary