ClearanceBrief
510(k) K211801 ยท NHI Stimulator, Nerve, Electrical, Percutaneous (Pens), For Pain Relief

SPRINT PNS System

ApplicantSpr Therapeutics, Inc., Cleveland OH, US
DecisionSubstantially Equivalent, Oct 13, 2021
ReceivedJun 10, 2021
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K211801

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.