The following data is part of a premarket notification filed by Ethicon, Inc. with the FDA for Vicryl Mesh.
| Device ID | K201143 |
| 510k Number | K201143 |
| Device Name: | VICRYL Mesh |
| Classification | Mesh, Surgical, Polymeric |
| Applicant | Ethicon, Inc. Route 22 West, P.O. Box 151 Somerville, NJ 08876 -0151 |
| Contact | Valerie Smith Beyer |
| Correspondent | Valerie Smith Beyer Ethicon, Inc. Route 22 West, P.O. Box 151 Somerville, NJ 08876 -0151 |
| Product Code | FTL |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2020-04-29 |
| Decision Date | 2020-08-06 |