Cleared Traditional

K883036 - PALLIAG NF III

K883036 is the FDA 510(k) clearance for PALLIAG NF III by Degussa Dental, Inc.. It is a Class 2 Dental device (product code EJT) cleared through the Traditional 510(k) pathway after a 24-day FDA review.

K883036 · Degussa Dental, Inc. · Dental device
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Aug 1988
Decision
24d
Days
Class 2
Risk

K883036 is an FDA 510(k) clearance for the PALLIAG NF III. Classified as Alloy, Gold-based Noble Metal (product code EJT), Class II - Special Controls.

Submitted by Degussa Dental, Inc. (Long Island, US). The FDA issued a Cleared decision on August 12, 1988 after a review of 24 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 Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Degussa Dental, Inc. devices

Submission Details

510(k) Number K883036 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 19, 1988
Decision Date August 12, 1988
Days to Decision 24 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
103d faster than avg
Panel avg: 127d · This submission: 24d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 436
Devices cleared under the same product code (EJT) and FDA review panel - the closest regulatory comparables to K883036.
ARGEDENT 52SF
K891911 · Argen Precious Metals, Inc. · May 1989
ULTIMA LITE
K890568 · Deringer-Ney, Inc. · Mar 1989
NEYORO 65CF
K890569 · Deringer-Ney, Inc. · Mar 1989
JEL-5 GOLD BASED ALLOYS & PRECIOUS METAL ALLOYS
K882126 · J.F. Jelenko & Co., Inc. · Jun 1988
OLYMPIA II
K881860 · J.F. Jelenko & Co., Inc. · Jun 1988
PTM-45
K881861 · J.F. Jelenko & Co., Inc. · Jun 1988