Cleared Traditional

K800994 - AUSTRY ALLOY(DENTAL BAKE-ON ALLOY)

K800994 is the FDA 510(k) clearance for AUSTRY ALLOY(DENTAL BAKE-ON ALLOY) by Howmedica Corp.. It is a Class 2 Dental device (product code EJS) cleared through the Traditional 510(k) pathway after a 7-day FDA review.

K800994 · Howmedica Corp. · Dental device
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May 1980
Decision
7d
Days
Class 2
Risk

K800994 is an FDA 510(k) clearance for the AUSTRY ALLOY(DENTAL BAKE-ON ALLOY). Classified as Alloy, Other Noble Metal (product code EJS), Class II - Special Controls.

Submitted by Howmedica Corp. (Mchenry, US). The FDA issued a Cleared decision on May 2, 1980 after a review of 7 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 Howmedica Corp. devices

Submission Details

510(k) Number K800994 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 25, 1980
Decision Date May 02, 1980
Days to Decision 7 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
120d faster than avg
Panel avg: 127d · This submission: 7d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EJS Alloy, Other 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 - EJS Alloy, Other Noble Metal

All 110
Devices cleared under the same product code (EJS) and FDA review panel - the closest regulatory comparables to K800994.
BAK-ON SP PORCELAIN ALLOY
K812101 · Johnson & Johnson Professionals, Inc. · Aug 1981
HOWMEDICA T-III G ALLOY
K810380 · Howmedica Corp. · Mar 1981
GDC 934
K801277 · Deringer-Ney, Inc. · Jul 1980
TEMPO
K792274 · Deringer-Ney, Inc. · Nov 1979
HOWMEDICA A-35 DENTAL ALLOY
K791973 · Howmedica Corp. · Nov 1979
HOWMEDICA AG-PD CROWN AND BRIDGE ALLOY
K792008 · Howmedica Corp. · Nov 1979