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SPRINT Peripheral Nerve Stimulation System, Extensa, SPRINT Peripheral Nerve Stimulation System, Endura, SPRINT Clinical Programmer Kit

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181422
510(k) Type
Traditional
Applicant
Spr Therapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2018
Days to Decision
61 days
Submission Type
Summary

SPRINT Peripheral Nerve Stimulation System, Extensa, SPRINT Peripheral Nerve Stimulation System, Endura, SPRINT Clinical Programmer Kit

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K181422
510(k) Type
Traditional
Applicant
Spr Therapeutics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2018
Days to Decision
61 days
Submission Type
Summary