ClearanceBrief
510(k) K831513 ยท HSX Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

KENNEDY TIBIAL COMPONENT

ApplicantBiomet, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jul 28, 1983
ReceivedMay 12, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K831513

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.