510(k) K081050 ยท FTL Mesh, Surgical, Polymeric
PARIETEX PROGRIP MESH
| Applicant | Sofradim Production, North Haven CT, US |
| Decision | Substantially Equivalent, May 28, 2008 |
| Received | Apr 14, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081050
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.