Cleared Traditional

K070124 - GASTROSTOMY REPLACEMENT TUBE, MODEL 253

K070124 is an FDA 510(k) clearance for GASTROSTOMY REPLACEMENT TUBE, manufactured by Degania Silicone , Ltd.. The device is a Class 2 Gastroenterology & Urology device with product code KNT cleared through the Traditional 510(k) pathway after a 127-day FDA review.

K070124 · Degania Silicone , Ltd. · Gastroenterology & Urology device
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May 2007
Decision
127d
Days
Class 2
Risk

K070124 is an FDA 510(k) clearance for the GASTROSTOMY REPLACEMENT TUBE, MODEL 253. Classified as Tubes, Gastrointestinal (and Accessories) (product code KNT), Class II - Special Controls.

Submitted by Degania Silicone , Ltd. (Emek Hayarden, IL). The FDA issued a Cleared decision on May 23, 2007 after a review of 127 days - within the typical 510(k) review window.

This device falls under the Gastroenterology & Urology FDA review panel, regulated under 21 CFR 876.5980 - 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 Degania Silicone , Ltd. devices

FDA 510(k) Submission Details - K070124

510(k) Number K070124 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 16, 2007
Decision Date May 23, 2007
Days to Decision 127 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
4d faster than avg
Panel avg: 131d · This submission: 127d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KNT Device Classification - Class 2, Special Controls

Product Code KNT Tubes, Gastrointestinal (and Accessories)
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 876.5980
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 - KNT Tubes, Gastrointestinal (and Accessories)

All 475
Devices cleared under the same product code (KNT) and FDA review panel - the closest regulatory comparables to K070124.
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K063061 · Viasys Medsystems · Apr 2007
BARD BALLOON DILATION KIT WITH TRIFUNNEL GASTROSTOMY TUBE
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K061432 · Hospira, Inc. · Sep 2006