510(k) K031925 ยท FTL Mesh, Surgical, Polymeric
PROCEED TRILAMINATE SURGICAL MESH
| Applicant | ETHICON, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, Sep 17, 2003 |
| Received | Jun 23, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K031925
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 26, 2006 | Ethicon, Inc. PROCEED Surgical Mesh is a sterile, thin, flexible laminate mesh designed for the repair of hernias and other fascial deficiencies. The mesh product is comprised of an oxidized regenerated cellulose Terminated |
FTL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.