ClearanceBrief
510(k) K071220 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

COLUMBUS TOTAL KNEE SYSTEM AS

ApplicantAesculap Implant Systems, Inc., Center Valley PA, US
DecisionSubstantially Equivalent, Jun 1, 2007
ReceivedMay 2, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K071220

DateFirm and productCodeLinked 510(k)
Jan 21, 2020Aesculap Implant Systems LLC
AS COLUMBUS CR/PS TIB.PLAT.CEMENTED,Knee implant components, various sizes, model nos. NN058Z NN070Z NN071Z NN072Z NN073Z NN074Z NN075Z NN076Z NN077Z NN078Z NN079Z NN470Z NN471Z NN472Z NN473Z NN474Z
Terminated
JWHNone listed

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