ClearanceBrief
510(k) K180653 ยท HCG Device, Neurovascular Embolization

Spartan eCoil System

ApplicantSpartan Micro, Inc., Fremont CA, US
DecisionSubstantially Equivalent, Dec 4, 2018
ReceivedMar 13, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K180653

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.