The following data is part of a premarket notification filed by Cook Incorporated with the FDA for Greene Renal Transplant Stent Set.
Device ID | K180557 |
510k Number | K180557 |
Device Name: | Greene Renal Transplant Stent Set |
Classification | Stent, Ureteral |
Applicant | Cook Incorporated 750 Daniels Way Bloomington, IN 47404 |
Contact | Yuan Zhou |
Correspondent | Yuan Zhou Cook Incorporated 750 Daniels Way Bloomington, IN 47404 |
Product Code | FAD |
CFR Regulation Number | 876.4620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-03-01 |
Decision Date | 2018-11-23 |
Summary: | summary |