ClearanceBrief
510(k) K002677 ยท BXM Stimulator, Nerve, Ac-Powered

NUVASIVE INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM

ApplicantNuvasive, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Nov 13, 2000
ReceivedAug 28, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K002677

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.