ClearanceBrief
510(k) K926228 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

DURACON CRUCIFORM TIBIAL BASEPLATE

ApplicantHowmedica Corp., Rutherford NJ, US
DecisionSubstantially Equivalent, Feb 22, 1994
ReceivedDec 11, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K926228

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.