The following data is part of a premarket notification filed by Cook Ireland Ltd with the FDA for Zilver 518 Biliary Stent, Zilver 635 Biliary Stent.
| Device ID | K182980 |
| 510k Number | K182980 |
| Device Name: | Zilver 518 Biliary Stent, Zilver 635 Biliary Stent |
| Classification | Stents, Drains And Dilators For The Biliary Ducts |
| Applicant | Cook Ireland Ltd O' Halloran Rd, National Technology Park Limerick, IE |
| Contact | Cathrina Mchale |
| Correspondent | Cathrina Mchale Cook Ireland Ltd O' Halloran Rd, National Technology Park Limerick, IE |
| Product Code | FGE |
| CFR Regulation Number | 876.5010 [🔎] |
| Decision | Se - With Limitations (SESU) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-10-29 |
| Decision Date | 2018-11-16 |
| Summary: | summary |