ClearanceBrief
510(k) K202781 ยท GZF Stimulator, Peripheral Nerve, Implanted (Pain Relief)

Neuspera Neurostimulation System (NNS)

ApplicantNeuspera Medical, Inc., San Jose CA, US
DecisionSubstantially Equivalent, Aug 27, 2021
ReceivedSep 22, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K202781

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.