510(k) K083102 ยท FTL Mesh, Surgical, Polymeric
REFINE LIFT SYSTEM
| Applicant | Alure Medical, Inc., Carlsbad CA, US |
| Decision | Substantially Equivalent, May 11, 2009 |
| Received | Oct 20, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083102
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.