Cleared Traditional

K933083 - DW247 #2

K933083 is an FDA 510(k) clearance for DW247 #2, manufactured by Ivoclar North America, Inc.. The device is a Class 2 Dental device with product code EJT cleared through the Traditional 510(k) pathway after a 98-day FDA review.

K933083 · Ivoclar North America, Inc. · Dental device
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Sep 1993
Decision
98d
Days
Class 2
Risk

K933083 is an FDA 510(k) clearance for the DW247 #2. Classified as Alloy, Gold-based Noble Metal (product code EJT), Class II - Special Controls.

Submitted by Ivoclar North America, Inc. (Amherst, US). The FDA issued a Cleared decision on September 29, 1993 after a review of 98 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3060 - the FDA dental device regulatory 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 Dental review framework, consistent with the majority of Class II 510(k) submissions.

View all Ivoclar North America, Inc. devices

FDA 510(k) Submission Details - K933083

510(k) Number K933083 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 23, 1993
Decision Date September 29, 1993
Days to Decision 98 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
29d faster than avg
Panel avg: 127d · This submission: 98d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 551
Devices cleared under the same product code (EJT) and FDA review panel - the closest regulatory comparables to K933083.
ARGENCO M
K931556 · Argen Precious Metals, Inc. · Dec 1993
ARGELITE W
K934769 · Argen Precious Metals, Inc. · Nov 1993
GDC 3509
K933178 · Deringer-Ney, Inc. · Oct 1993
DW 248 #46
K933186 · Ivoclar North America, Inc. · Sep 1993
ARGELITE 85
K931554 · Argen Precious Metals, Inc. · Jul 1993
ARGELITE 55
K931475 · Argen Precious Metals, Inc. · Jul 1993