ClearanceBrief
510(k) K910877 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

FINN KNEE PROSTHESIS

ApplicantBiomet, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Jul 26, 1991
ReceivedMar 1, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910877

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.