ClearanceBrief
510(k) K090907 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)

PENTA LEAD KITS, MODELS: 3227-3234

ApplicantAdvanced Neuromodulation Systems, Plano TX, US
DecisionSubstantially Equivalent, Jun 2, 2009
ReceivedApr 1, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090907

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.