510(k) K071887 ยท FTL Mesh, Surgical, Polymeric
SPORTMESH OR ARTELON TISSUE REINFORCEMENT
| Applicant | Artimplant AB, Washington DC, US |
| Decision | Substantially Equivalent, Sep 18, 2007 |
| Received | Jul 9, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071887
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.