510(k) K172017
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)