510(k) K113311 ยท FTL Mesh, Surgical, Polymeric
TIO2MESH TM
| Applicant | Biocer Entwicklungs GmbH, Austin TX, US |
| Decision | Substantially Equivalent, Jul 17, 2012 |
| Received | Nov 9, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113311
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.