ClearanceBrief
510(k) K070707 ยท HCG Device, Neurovascular Embolization

MICRUS MICROCOIL SYSTEM

ApplicantMicrus Endovascular Corporation, San Jose CA, US
DecisionSubstantially Equivalent, Apr 6, 2007
ReceivedMar 14, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K070707

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.