ClearanceBrief
510(k) K090298 ยท GWF Stimulator, Electrical, Evoked Response

NUVASIVE NEURO VISION SYSTEM

ApplicantNuvasive, Inc., San Diego CA, US
DecisionSubstantially Equivalent, Jun 8, 2009
ReceivedFeb 6, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090298

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.