ClearanceBrief
510(k) K982160 ยท KRO Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer

HINGED KNEE

ApplicantEncore Orthopedics, Inc., Austin TX, US
DecisionSubstantially Equivalent, Mar 17, 1999
ReceivedJun 19, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K982160

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.