510(k) K172017

Black Silicone Filiform Double Pigtail Stent Set by Cook Incorporated — Product Code FAD

K172017 is an FDA 510(k) premarket notification submitted by Cook Incorporated for the device "Black Silicone Filiform Double Pigtail Stent Set". The FDA issued a decision of Substantially Equivalent - Kit on Mar 26, 2018. The device falls under product code FAD (Stent, Ureteral), a Class II device regulated under 21 CFR 876.4620. Cook Incorporated has 174 other 510(k) clearances on record.

Clearance Details

Decision
SESK (Substantially Equivalent - Kit)
Decision Date
Mar 26, 2018
Date Received
Jul 3, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stent, Ureteral
Device Class
Class II
Regulation Number
876.4620
Review Panel
GU
Submission Type
510(k)