ClearanceBrief
510(k) K072462 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)

WIDE SPACED QUATTRODE LEADS

ApplicantAdvanced Neuromodulation Systems, Plano TX, US
DecisionSubstantially Equivalent, Oct 11, 2007
ReceivedAug 31, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K072462

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.