510(k) K060713 ยท FTL Mesh, Surgical, Polymeric
PROCEED SURGICAL MESH
| Applicant | ETHICON, Inc., Somerville NJ, US |
| Decision | Substantially Equivalent, May 25, 2006 |
| Received | Mar 17, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060713
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 23, 2020 | Ethicon, Inc. PROCEED Surgical Mesh
Hernia Mesh Oval, 15 cm x 20 cm Terminated |
FTL | None listed |
| Apr 3, 2014 | Ethicon, Inc. Proceed Surgical Mesh, Product Codes PCDB1, PCDT1, and PCDJ1.
Ethicon Inc., Johnson & Johnson Medical GmbH, used for the repair of hernias and other fascial deficiencies that require the addition Open, Classified |
FTM | None listed |
| Jan 14, 2011 | Ethicon, Inc. PROCEED Surgical Mesh; Product Code PCDG1; :Lot BMG618; Ethicon, Inc. a Johnson & Johnson Company.
Used for the repair of hernias and other fascial deficiencies that require the addition of a reinfor Open, Classified |
FTL | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.