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Receiver Kit, Trial Kit, Spare Lead Kit, Sterile Revision Kit, SWAG Kit, SWAG Accessory Kit, Charger Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171366
510(k) Type
Traditional
Applicant
Stimwave Technologies Inc.,DBA StimQ LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2017
Days to Decision
87 days
Submission Type
Summary

Receiver Kit, Trial Kit, Spare Lead Kit, Sterile Revision Kit, SWAG Kit, SWAG Accessory Kit, Charger Kit

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K171366
510(k) Type
Traditional
Applicant
Stimwave Technologies Inc.,DBA StimQ LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/2017
Days to Decision
87 days
Submission Type
Summary