510(k) K041106 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
REVISION KNEE SYSTEM
| Applicant | Smith & Nephew, Inc., Memphis TN, US |
| Decision | Substantially Equivalent, Jul 1, 2004 |
| Received | Apr 28, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K041106
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 14, 2017 | Smith & Nephew, Inc. smith&nephew LEGION L-WEDGE, 10 MM DIS X 5 MM POS, SIZE 4, SCREW-ON FEMORAL WEDGE, REF 71421733, STERILE R
Product The Revision Knee System Components are indicated for rheumatoid arthritis; post-tra Terminated |
JWH | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.