Cleared Traditional

K900269 - PORGES DORMIA 3 FR FLAT WIRE BASKET STONE DISLODGE

K900269 is an FDA 510(k) clearance for PORGES DORMIA 3 FR FLAT WIRE BASKET STO..., manufactured by Porges Corp.. The device is a Class 2 Gastroenterology & Urology device with product code FFL cleared through the Traditional 510(k) pathway after a 166-day FDA review.

K900269 · Porges Corp. · Gastroenterology & Urology device
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Jul 1990
Decision
166d
Days
Class 2
Risk

K900269 is an FDA 510(k) clearance for the PORGES DORMIA 3 FR FLAT WIRE BASKET STONE DISLODGE. Classified as Dislodger, Stone, Basket, Ureteral, Metal (product code FFL), Class II - Special Controls.

Submitted by Porges Corp. (Gary, US). The FDA issued a Cleared decision on July 3, 1990 after a review of 166 days - an extended review cycle.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.4680 - 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 Porges Corp. devices

FDA 510(k) Submission Details - K900269

510(k) Number K900269 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 18, 1990
Decision Date July 03, 1990
Days to Decision 166 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
35d slower than avg
Panel avg: 131d · This submission: 166d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

FFL Device Classification - Class 2, Special Controls

Product Code FFL Dislodger, Stone, Basket, Ureteral, Metal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.4680
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 - FFL Dislodger, Stone, Basket, Ureteral, Metal

All 43
Devices cleared under the same product code (FFL) and FDA review panel - the closest regulatory comparables to K900269.
LOOP RETRIEVER
K922678 · Annex Medical, Inc. · Aug 1992
BARD 4-WIRE URETEROSCOPIC STONE
K921233 · C.R. Bard, Inc. · Apr 1992
LOOP RETRIEVER
K910603 · Annex Medical, Inc. · Mar 1991
METAL URETERAL BASKET STONE DISLODGER
K896992 · Annex Medical, Inc. · Feb 1990
METAL URETERAL BASKET STONE DISLODGER
K896169 · Annex Medical, Inc. · Dec 1989
CANDELA STONE BASKETS
K884738 · Candela Laser Corp. · Feb 1989