ClearanceBrief
510(k) K072800 ยท MCW Catheter, Peripheral, Atherectomy

DIAMONDBACK 360 DEGREE ORBITAL ATHERECTOMY SYSTEM

ApplicantCardiovascular Systems, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Oct 25, 2007
ReceivedOct 1, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K072800

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.