510(k) K024022 ยท HXN Applier, Cerclage
OSTEO-CABLE SLEEVE
| Applicant | Biomet, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Jan 23, 2003 |
| Received | Dec 5, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K024022
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.