ClearanceBrief
510(k) K071246 ยท HCG Device, Neurovascular Embolization

MICRUS MICROCOIL DELIVERY SYSTEM, MODELS SPH, HEL, CHE, PC4, HSR, FSR, CSP, CFS, SRC, PP4, STR

ApplicantMicrus Endovascular Corporation, San Jose CA, US
DecisionSubstantially Equivalent, Jun 1, 2007
ReceivedMay 3, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K071246

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.