ClearanceBrief
510(k) K960356 ยท KRH Ring, Annuloplasty

POSTERIOR ANNULOPLASTY BAND (MODEL 607)

ApplicantThe Heart Valve Div. Medtronic Cardiovascular Surg, Irvine CA, US
DecisionSubstantially Equivalent - Subject to Tracking Reg., Aug 27, 1996
ReceivedJan 25, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960356

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.