Cleared Abbreviated

K021741 - CRITERTION, MODEL #1067511

K021741 is an FDA 510(k) clearance for CRITERTION, manufactured by Sterngold. The device is a Class 2 Dental device with product code EJT cleared through the Abbreviated 510(k) pathway after a 29-day FDA review.

K021741 · Sterngold · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 2002
Decision
29d
Days
Class 2
Risk

K021741 is an FDA 510(k) clearance for the CRITERTION, MODEL #1067511. Classified as Alloy, Gold-based Noble Metal (product code EJT), Class II - Special Controls.

Submitted by Sterngold (Attleboro, US). The FDA issued a Cleared decision on June 26, 2002 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3060 - the FDA dental device regulatory framework. The Abbreviated 510(k) pathway was used, relying on FDA-recognized standards to demonstrate substantial equivalence.

Device pattern: Standards-based predicate clearance. Standards-verified equivalence. The Abbreviated pathway signals strong alignment with FDA-recognized performance standards - typically associated with lower review burden and faster clearance cycles.

View all Sterngold devices

FDA 510(k) Submission Details - K021741

510(k) Number K021741 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 28, 2002
Decision Date June 26, 2002
Days to Decision 29 days
Submission Type Abbreviated
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
98d faster than avg
Panel avg: 127d · This submission: 29d
Pathway characteristics
Standards-based clearance path.

EJT Device Classification - Class 2, Special Controls

Product Code EJT Alloy, Gold-based Noble Metal
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3060
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 Dental devices follow this clearance model.

Regulatory Peers - EJT Alloy, Gold-based Noble Metal

All 544
Devices cleared under the same product code (EJT) and FDA review panel - the closest regulatory comparables to K021741.
BRIGHT GOLD
K021892 · Ivoclar Vivadent, Inc. · Jul 2002
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K021926 · Wieland Dental + Technik GmbH & Co. KG · Jul 2002
AUTOPAL 50
K021733 · Wieland Dental + Technik GmbH & Co. KG · Jun 2002
PORTALLOY 54
K021242 · Wieland Dental + Technik GmbH & Co. KG · May 2002
PORTADUR P 4
K020190 · Wieland Dental + Technik GmbH & Co. KG · Mar 2002
GPW-SF
K011659 · Gateway Alloys, Inc. · Aug 2001