ClearanceBrief
510(k) K823420 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

KINEMATIC II KNEE SYSTEM

ApplicantHowmedica Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 7, 1983
ReceivedNov 15, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823420

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.