ClearanceBrief
510(k) K153053 ยท MOF Guide, Wire, Catheter, Neurovasculature

Traxcess Pro 14 Guidewire

ApplicantMicroVention, Inc., Tustin CA, US
DecisionSubstantially Equivalent, Dec 29, 2015
ReceivedOct 20, 2015
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K153053

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.