The following data is part of a premarket notification filed by Synovis Surgical Innovations with the FDA for Peri-strips Staple Line Reinforcement-sleeve Configuration, Peri-strips Staple Line Reinforcement-strip Configuration.
| Device ID | K040119 |
| 510k Number | K040119 |
| Device Name: | PERI-STRIPS STAPLE LINE REINFORCEMENT-SLEEVE CONFIGURATION, PERI-STRIPS STAPLE LINE REINFORCEMENT-STRIP CONFIGURATION |
| Classification | Mesh, Surgical |
| Applicant | SYNOVIS SURGICAL INNOVATIONS 2575 UNIVERSITY AVE. St. Paul, MN 55114 -1024 |
| Contact | Angela Mallery |
| Correspondent | Angela Mallery SYNOVIS SURGICAL INNOVATIONS 2575 UNIVERSITY AVE. St. Paul, MN 55114 -1024 |
| Product Code | FTM |
| CFR Regulation Number | 878.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-01-20 |
| Decision Date | 2004-03-17 |
| Summary: | summary |