510(k) K070961 ยท FTL Mesh, Surgical, Polymeric
BIOMERIX SURGICAL MESH, MODEL: RCR-01
| Applicant | Biomerix Corporation, Rockville MD, US |
| Decision | Substantially Equivalent, Feb 25, 2008 |
| Received | Apr 5, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070961
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.