ClearanceBrief
510(k) K030118 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)

RAPID PROGRAMMAR

ApplicantAdvanced Neuromodulation Systems, Plano TX, US
DecisionSubstantially Equivalent, Mar 11, 2003
ReceivedJan 13, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K030118

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.