510(k) K020989 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented
SUPER EON PLUS FEMORAL STEMS
| Applicant | Howmedica Osteonics Corp., Allendale NJ, US |
| Decision | Substantially Equivalent, Apr 26, 2002 |
| Received | Mar 27, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020989
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 26, 2009 | Stryker Howmedica Osteonics Corp. Japanese Omnifit Eon 127 NK
These devices are modular components of a total hip system. These femoral stems are intended for use with femoral heads and acetabular components in primary or revision to Terminated |
JDI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.