ClearanceBrief
510(k) K923931 ยท GZB Stimulator, Spinal-Cord, Implanted (Pain Relief)

MEDTRONIC MODEL 3487A PISCES-QUAD LEAD

ApplicantMedtronic Vascular, Minneapolis MN, US
DecisionSubstantially Equivalent, Mar 18, 1993
ReceivedAug 5, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K923931

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.