510(k) K062915 ยท FTM Mesh, Surgical
VERITAS COLLAGEN MATRIX
| Applicant | Synovis Surgical Innovations, St. Paul MN, US |
| Decision | Substantially Equivalent, Dec 6, 2006 |
| Received | Sep 27, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062915
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 11, 2020 | Baxter Healthcare Corporation VERITAS Collagen Matrix - Product Usage: intended for use in reconstruction of the pelvic floor excluding transvaginal pelvic organ prolapse and for use in the repair of rectal prolapse excluding rect Terminated |
FTM | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.