Cleared Traditional

K260196 - ETHICON™ Circular Stapler (CDH21mm) (FDA 510(k) Clearance)

Also includes:
ETHICON™ Circular Stapler (CDH25mm) ETHICON™ Circular Stapler (CDH29mm) ETHICON™ Circular Stapler (CDH33mm) ETHICON™ Circular Stapler - XL Sealed (ECS21mm) ETHICON™ Circular Stapler - XL Sealed (ECS25mm) ETHICON™ Circular Stapler - XL Sealed (ECS29mm) ETHICON™ Circular Stapler - XL Sealed (ECS33mm)

Class II General & Plastic Surgery device cleared through predicate-based substantial equivalence - typically does not require clinical trials.

K260196 · Ethicon Endo-Surgery, LLC · General & Plastic Surgery device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
May 2026
Decision
109d
Days
Class 2
Risk

K260196 is an FDA 510(k) clearance for the ETHICON™ Circular Stapler (CDH21mm). Classified as Staple, Implantable (product code GDW), Class II - Special Controls.

Submitted by Ethicon Endo-Surgery, LLC (Guaynabo, US). The FDA issued a Cleared decision on May 11, 2026 after a review of 109 days - within the typical 510(k) review window.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.4750 - the FDA general and plastic surgery 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 General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Ethicon Endo-Surgery, LLC devices

Submission Details

510(k) Number K260196 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 22, 2026
Decision Date May 11, 2026
Days to Decision 109 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
5d faster than avg
Panel avg: 114d · This submission: 109d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code GDW Staple, Implantable
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.4750
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 General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GDW Staple, Implantable

All 282
Devices cleared under the same product code (GDW) and FDA review panel - the closest regulatory comparables to K260196.
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K243276 · Ethicon Endo-Surgery, LLC · Feb 2025
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K241630 · Ethicon Endo-Surgery, LLC · Oct 2024
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