ClearanceBrief
510(k) K240871 ยท MOF Guide, Wire, Catheter, Neurovasculature

Synxess Neurovascular Guidewire

ApplicantEnlight Medical Technologies (Shenzhen) Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Nov 18, 2024
ReceivedMar 29, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K240871

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.