ClearanceBrief
510(k) K874919 ยท JDQ Cerclage, Fixation

ORTHOMET WIRE FOR SUTURE, CERCLAGE

ApplicantOrthomet, Inc., Minneapolis MN, US
DecisionSubstantially Equivalent, Jan 7, 1988
ReceivedDec 3, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K874919

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.