The following data is part of a premarket notification filed by Cordis Corp. with the FDA for Modification To Cordis Palmaz Genesis Transhepatic Biliary Stent.
| Device ID | K020809 |
| 510k Number | K020809 |
| Device Name: | MODIFICATION TO CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT |
| Classification | Stents, Drains And Dilators For The Biliary Ducts |
| Applicant | CORDIS CORP. 7 POWDER HORN DR. Warren, NJ 07059 |
| Contact | Donna Marshall |
| Correspondent | Donna Marshall CORDIS CORP. 7 POWDER HORN DR. Warren, NJ 07059 |
| Product Code | FGE |
| CFR Regulation Number | 876.5010 [🔎] |
| Decision | Se - With Limitations (SESU) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2002-03-13 |
| Decision Date | 2002-04-12 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 20705032057582 | K020809 | 000 |
| 20705032057544 | K020809 | 000 |
| 20705032057506 | K020809 | 000 |
| 20705032057490 | K020809 | 000 |
| 20705032057452 | K020809 | 000 |