The following data is part of a premarket notification filed by Sofradim Production with the FDA for Sofradim Parietex Surgical Meshes.
| Device ID | K003990 |
| 510k Number | K003990 |
| Device Name: | SOFRADIM PARIETEX SURGICAL MESHES |
| Classification | Mesh, Surgical, Polymeric |
| Applicant | SOFRADIM PRODUCTION 5 WHITCOMB AVENUE Ayer, MA 01432 |
| Contact | Mary Mcnamara-cullinane |
| Correspondent | Mary Mcnamara-cullinane SOFRADIM PRODUCTION 5 WHITCOMB AVENUE Ayer, MA 01432 |
| Product Code | FTL |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-12-26 |
| Decision Date | 2001-01-24 |