ClearanceBrief
510(k) K820030 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer

HOWMEDICA KINEMATIC TOTAL CONDYLAR KNEE

ApplicantHowmedica Corp., Walker MI, US
DecisionSubstantially Equivalent, Feb 5, 1982
ReceivedJan 5, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820030

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.