ClearanceBrief
510(k) K053250 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)

ANS 90 CM AND 110 CM (3100 AND 3200 SERIES) LEAD KIT

ApplicantAdvanced Neuromodulation Systems, Plano TX, US
DecisionSubstantially Equivalent, Dec 15, 2005
ReceivedNov 21, 2005
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K053250

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.