ClearanceBrief
510(k) K181422 ยท NHI Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief

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

ApplicantSpr Therapeutics, Inc., Cleveland OH, US
DecisionSubstantially Equivalent, Jul 31, 2018
ReceivedMay 31, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K181422

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.