510(k) K002233 ยท PAJ Mesh, Surgical, Non-Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally Placed
BVI SLING
| Applicant | Bio-Vascular, Inc., St. Paul MN, US |
| Decision | Substantially Equivalent, Oct 13, 2000 |
| Received | Jul 24, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002233
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 11, 2002 | Synovis Surgical Inovation Div. of Surgical Mesh Terminated |
79F | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.