The following data is part of a premarket notification filed by Tepha, Inc. with the FDA for Tephaflex Absorbable Suture.
| Device ID | K081099 |
| 510k Number | K081099 |
| Device Name: | TEPHAFLEX ABSORBABLE SUTURE |
| Classification | Suture, Recombinant Technology |
| Applicant | TEPHA, INC. 99 HAYDEN, SUTIE 360 Lexington, MA 02421 |
| Contact | Mary P Legraw |
| Correspondent | Mary P Legraw TEPHA, INC. 99 HAYDEN, SUTIE 360 Lexington, MA 02421 |
| Product Code | NWJ |
| CFR Regulation Number | 878.4494 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-04-17 |
| Decision Date | 2008-07-15 |
| Summary: | summary |