510(k) K212431 ยท JDG Prosthesis, Hip, Femoral Component, Cemented, Metal
Biomet Answer/Impact/Integral Distal Centralizer/Centering Sleeve
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Feb 7, 2022 |
| Received | Aug 4, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K212431
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.