510(k) K081882 ยท FTM Mesh, Surgical
MODIFICATION TO XYLOS SURGICAL MESH
| Applicant | Xylos Corporation, Langhorne PA, US |
| Decision | Substantially Equivalent, Jul 11, 2008 |
| Received | Jul 2, 2008 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K081882
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.