510(k) K942479 ยท JDG Prosthesis, Hip, Femoral Component, Cemented, Metal
INTEGRAL CO-CR FEMORAL COMPONENT
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Sep 20, 1994 |
| Received | May 25, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942479
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 13, 2016 | Biomet, Inc. Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo),
9mm, 11mm, 13mm, 15mm, and 17mm Terminated |
LZO | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.