The following data is part of a premarket notification filed by Tepha, Inc. with the FDA for Tephaflex Mesh.
| Device ID | K113723 |
| 510k Number | K113723 |
| Device Name: | TEPHAFLEX MESH |
| Classification | Surgical Film |
| Applicant | TEPHA, INC. 99 HAYDEN, SUITE 360 Lexington, MA 02421 |
| Contact | Mary P Legraw |
| Correspondent | Mary P Legraw TEPHA, INC. 99 HAYDEN, SUITE 360 Lexington, MA 02421 |
| Product Code | OOD |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-12-19 |
| Decision Date | 2012-02-15 |
| Summary: | summary |