510(k) K921139 ยท JDL Prosthesis, Hip, Semi-Constrained (Metal Cemented Acetabular Component)
HEALEY REVISION COMPONENT SYSTEM
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jul 1, 1992 |
| Received | Mar 10, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921139
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.