510(k) K103682 ยท FTL Mesh, Surgical, Polymeric
PARIETEX PROGRIP
| Applicant | Sofradim Production, Bedford MA, US |
| Decision | Substantially Equivalent, Mar 4, 2011 |
| Received | Dec 17, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103682
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.