510(k) K052830 ยท FTL Mesh, Surgical, Polymeric
SPORTMESH
| Applicant | Artimplant AB, Washington DC, US |
| Decision | Substantially Equivalent, Jan 19, 2006 |
| Received | Oct 5, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052830
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.