510(k) K082941 ยท FTL Mesh, Surgical, Polymeric
BIOMERIX COMPOSITE SURGICAL MESH, MODEL SMNR-0510 AND SMNR-1215
| Applicant | Biomerix Corporation, Fremont CA, US |
| Decision | Substantially Equivalent, Jan 7, 2009 |
| Received | Oct 2, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082941
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.