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 |