ClearanceBrief
510(k) K013215 ยท BXM Stimulator, Nerve, Ac-Powered

MODIFIED INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM

ApplicantNuvasive, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Oct 16, 2001
ReceivedSep 26, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K013215

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.