Cleared Traditional

K172017 - Black Silicone Filiform Double Pigtail ...

K172017 is an FDA 510(k) clearance for Black Silicone Filiform Double Pigtail ..., manufactured by Cook Incorporated. The device is a Class 2 Gastroenterology & Urology device with product code FAD cleared through the Traditional 510(k) pathway after a 266-day FDA review.

K172017 · Cook Incorporated · Gastroenterology & Urology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2018
Decision
266d
Days
Class 2
Risk

K172017 is an FDA 510(k) clearance for the Black Silicone Filiform Double Pigtail Stent Set. Classified as Stent, Ureteral (product code FAD), Class II - Special Controls.

Submitted by Cook Incorporated (Bloomington, US). The FDA issued a Cleared decision on March 26, 2018 after a review of 266 days - an extended review cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.4620 - the FDA gastroenterology and urology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Gastroenterology & Urology review framework, consistent with the majority of Class II 510(k) submissions.

View all Cook Incorporated devices

FDA 510(k) Submission Details - K172017

510(k) Number K172017 FDA.gov
FDA Decision Cleared Substantially Equivalent - Special 510(k) (SESK)
Date Received July 03, 2017
Decision Date March 26, 2018
Days to Decision 266 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
136d slower than avg
Panel avg: 130d · This submission: 266d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FAD Device Classification - Class 2, Special Controls

Product Code FAD Stent, Ureteral
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.4620
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Gastroenterology & Urology devices follow this clearance model.

Regulatory Peers - FAD Stent, Ureteral

All 96
Devices cleared under the same product code (FAD) and FDA review panel - the closest regulatory comparables to K172017.
Malecot Nephrostomy Catheter/Stent Set
K180029 · Cook Incorporated · Sep 2018
Sof-Flex Ureteral Stent Set
K180053 · Cook Incorporated · Sep 2018
Cope Nephroureterostomy Stent and Amplatz Ureteral Stent Set
K171603 · Cook Incorporated · Apr 2018
RocaJJ Soft Stents
K173734 · Promepla Sam · Mar 2018
VORTEK URETERAL DOUBLE LOOP STENT
K180057 · Coloplast Corp. · Mar 2018
VORTEK HYDRO-COATED DOUBLE LOOP URETERAL STENTS
K170362 · Coloplast Corp. · Nov 2017