ClearanceBrief
510(k) K070134 ยท BXN Stimulator, Nerve, Battery-Powered

MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098

ApplicantStockert GmbH, Freiburg, B-W, DE
DecisionSubstantially Equivalent, Mar 22, 2007
ReceivedJan 16, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K070134

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.