ClearanceBrief
510(k) K113455 ยท NRY Catheter, Thrombus Retriever

SOLITAIRE FR REVASCULARIZATION DEVICE

ApplicantMicro Therapeutics Dba Ev3 Neurovascular, Irvine CA, US
DecisionSubstantially Equivalent, Mar 2, 2012
ReceivedNov 21, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113455

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.