510(k) K070018 ยท FTL Mesh, Surgical, Polymeric
UNIVERSAL SURGICAL MESH, MODEL 100
| Applicant | Generic Medical Device, Inc., Houston TX, US |
| Decision | Substantially Equivalent, Apr 27, 2007 |
| Received | Jan 3, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K070018
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.