ClearanceBrief
510(k) K120961 ยท NRY Catheter, Thrombus Retriever

TREVO RETRIEVER

ApplicantConcentric Medical, Inc., Mountain View CA, US
DecisionSubstantially Equivalent, Aug 3, 2012
ReceivedMar 30, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120961

DateFirm and productCodeLinked 510(k)
Dec 8, 2014Concentric Medical Inc
Trevo Pro 4 Stent Retriever, Model number 80021; U.S. Indications for use: The Trevo Retriever is intended to restore blood flow in the neurovasculature by removing thrombus in patients experiencing i
Terminated
NRYNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.