ClearanceBrief
510(k) K904208 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

KINEMAX SUPERSTABILIZER TOTAL KNEE SYSTEM

ApplicantHowmedica Corp., Rutherford NJ, US
DecisionSubstantially Equivalent, Apr 1, 1991
ReceivedSep 12, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K904208

DateFirm and productCodeLinked 510(k)
May 14, 2015Stryker Howmedica Osteonics Corp.
Kinemax Stem Extenders, 80 mm, Product Usage: Kinemax Cemented Stem Extenders are modular components designed to be mated with tibial baseplates or femoral components of the Modular Rotating Hinge (M
Terminated
JWHNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.