ClearanceBrief
510(k) K990469 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)

LAMITRODE LEADS

ApplicantAdvanced Neuromodulation Systems, Allen TX, US
DecisionSubstantially Equivalent, Jun 3, 1999
ReceivedFeb 16, 1999
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K990469

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.