ClearanceBrief
Company ยท US

Spr Therapeutics, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2016 to 2026. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
NHIStimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief6
SCNTemporarily Implanted Peripheral Nerve Stimulation System For Sustained Pain Relief1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 14, 2026K240974SPRINT PNS System
Spr Therapeutics, Inc.
SCN
Jan 25, 2023K223306SPRINT Peripheral Nerve Stimulation (PNS) System
Spr Therapeutics, Inc.
NHI
Oct 13, 2021K211801SPRINT PNS System
Spr Therapeutics, Inc.
NHI
Jan 22, 2021K202660SPRINT PNS System
Spr Therapeutics, Inc.
NHI
Jul 31, 2018K181422SPRINT Peripheral Nerve Stimulation System, Extensa, SPRINT Peripheral Nerve Stimulation System, Endura, SPRINT Clinical
Spr Therapeutics, Inc.
NHI
Jun 26, 2017K170902Sprint System, Single Procedure Kit, Sprint System with Pad II, Single Procedure Kit, Sprint System, Multi-Procedure Kit
Spr Therapeutics, LLC
NHI
Jul 23, 2016K161154Smartpatch PNS MicroLead and Accessories, Smartpatch PNS Stimulator, Pads, and Accessories, Smartpatch PNS MicroLead and
Spr Therapeutics, LLC
NHI

Latest recalls

DateFirm and productCodeLinked 510(k)
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