510(k) K093123 ยท FTL Mesh, Surgical, Polymeric
BIOMERIX VENTRAL HERNIA REPAIR MESH, MODEL SM3-TAB
| Applicant | Biomerix Corporation, Fremont CA, US |
| Decision | Substantially Equivalent, May 13, 2010 |
| Received | Oct 2, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093123
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.