ClearanceBrief
510(k) K230563 · KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

EVOLUTION® Hinge Knee System

ApplicantMicroport Orthopedics, Inc., Arlington TN, US
DecisionSubstantially Equivalent, Sep 27, 2023
ReceivedMar 1, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K230563

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.