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ThermoNeuroModulation Device, TNM Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN170023
510(k) Type
Direct
Applicant
Scion Neurostim, LLC
Country
United States
FDA Decision
Deleted
Decision Date
3/26/2018
Days to Decision
343 days

ThermoNeuroModulation Device, TNM Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
DEN170023
510(k) Type
Direct
Applicant
Scion Neurostim, LLC
Country
United States
FDA Decision
Deleted
Decision Date
3/26/2018
Days to Decision
343 days