510(k) K072370 ยท FTL Mesh, Surgical, Polymeric
SURGICRAFT SURGICAL MESH SYSTEM
| Applicant | Surgicraft , Ltd., Douglassville PA, US |
| Decision | Substantially Equivalent, Jul 24, 2008 |
| Received | Aug 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072370
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.