The following data is part of a premarket notification filed by Coloplast Corp with the FDA for Vortek Ureteral Double Loop Stent.
| Device ID | K180057 |
| 510k Number | K180057 |
| Device Name: | VORTEK URETERAL DOUBLE LOOP STENT |
| Classification | Stent, Ureteral |
| Applicant | Coloplast Corp 1601 West River Road North Minneapolis, MN 55411 |
| Contact | Cori Ragan |
| Correspondent | Cori Ragan Coloplast Corp 1601 West River Road North Minneapolis, MN 55411 |
| Product Code | FAD |
| CFR Regulation Number | 876.4620 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-01-08 |
| Decision Date | 2018-03-09 |
| Summary: | summary |