The following data is part of a premarket notification filed by Tepha, Inc. with the FDA for Tephaflex Surgical Film.
| Device ID | K072520 |
| 510k Number | K072520 |
| Device Name: | TEPHAFLEX SURGICAL FILM |
| Classification | Mesh, Surgical, Polymeric |
| Applicant | TEPHA, INC. 99 HAYDEN, SUTIE 360 Lexington, MA 02421 |
| Contact | Mary Legraw |
| Correspondent | Mary Legraw TEPHA, INC. 99 HAYDEN, SUTIE 360 Lexington, MA 02421 |
| Product Code | FTL |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-09-07 |
| Decision Date | 2007-11-29 |
| Summary: | summary |