510(k) K093912 ยท MBI Fastener, Fixation, Nondegradable, Soft Tissue
ARTHREX TIBIAL GRAFTBOLT
| Applicant | Arthrex, Inc., Naples FL, US |
| Decision | Substantially Equivalent, Mar 18, 2010 |
| Received | Dec 22, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093912
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.