510(k) K022204 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
VKS KNEE SYSTEM
| Applicant | Plus Orthopedics, San Diego CA, US |
| Decision | Substantially Equivalent, Oct 18, 2002 |
| Received | Jul 5, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022204
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 8, 2007 | Plus Orthopedics USA VKS PE Tibia Insert Ultra-Congruent; Left, Size 2, 12mm; Model Number: 0214612; Plus Orthopedics, San Diego, CA 92121 Terminated |
JWH | None listed |
| Jan 18, 2006 | Plus Orthopedics USA VKS Knee System; VKS Distal Femoral Resection Guide, Model Number 1214122, Revisions A and B. (Re-usable surgical instrument) Terminated |
JWH | None listed |
| Jun 22, 2005 | Plus Orthopedics USA Cancellous Bone Screw, 6.5 x 50 mm, Model 0214807 Terminated |
JWH | None listed |
| Feb 15, 2005 | Plus Orthopedics UltraCongruent Tibial Insert Model 0214703
Tibial Insert, Ultra-Congruent, Right, Size 3, 10mm Terminated |
JWH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.