ClearanceBrief
510(k) K063211 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

PROVEN KNEE SYSTEM HIGH FLEXION TIBIAL INSERT

ApplicantStelkast Company, Mcmurray PA, US
DecisionSubstantially Equivalent, Jan 18, 2007
ReceivedOct 23, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K063211

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.