510(k) K241000 · JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
ATTUNE Revision Knee System; DePuy Knee Prosthesis System Universal Stem Extensions and Universal Femoral Metaphyseal Sleeves; DePuy Sigma PS Femoral Components; DePuy Sigma Cruciate Retaining (C/R) Porocoat Femoral Components; S-ROM NOILES Rotating Hinge Knee System; DePuy P.F.C. SIGMA Total
| Applicant | Depuy Ireland UC, Ringaskiddy, Co. Cork, IE |
| Decision | Substantially Equivalent, Jul 11, 2024 |
| Received | Apr 12, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241000
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.