510(k) K022672 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
COLUMBUS TOTAL KNEE SYSTEM (CR)
| Applicant | Aesculap, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Nov 8, 2002 |
| Received | Aug 12, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022672
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 21, 2020 | Aesculap Implant Systems LLC Columbus R/PS TIB.PLATEAU Cemented, various sizes, Knee implant components, model nos. NN058K
NN070K
NN071K
NN072K
NN073K
NN074K
NN075K
NN076K
NN077K
NN078K
NN079K
Product Usage:Tibia-Plateaus are par Terminated |
JWH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.