510(k) K090271 ยท FTL Mesh, Surgical, Polymeric
HYDROCOAT MESH
| Applicant | Promethean Surgical Devices, Inc., East Harford CT, US |
| Decision | Substantially Equivalent, Jan 14, 2010 |
| Received | Feb 4, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K090271
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.