ClearanceBrief
510(k) K163154 ยท MOF Guide, Wire, Catheter, Neurovasculature

Traxcess 7 Mini XSoft Guidewire

ApplicantMicroVention, Inc., Tistin CA, US
DecisionSubstantially Equivalent, Dec 9, 2016
ReceivedNov 10, 2016
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K163154

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.