Cleared Traditional

K964773 - DENTEMP ONE STEP

K964773 is the FDA 510(k) clearance for DENTEMP ONE STEP by Majestic Drug Co., Inc.. It is a Class 2 Dental device (product code EMA) cleared through the Traditional 510(k) pathway after a 86-day FDA review.

K964773 · Majestic Drug Co., Inc. · Dental device
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Feb 1997
Decision
86d
Days
Class 2
Risk

K964773 is an FDA 510(k) clearance for the DENTEMP ONE STEP. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by Majestic Drug Co., Inc. (Bronx, US). The FDA issued a Cleared decision on February 21, 1997 after a review of 86 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3275 - 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 Majestic Drug Co., Inc. devices

Submission Details

510(k) Number K964773 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 27, 1996
Decision Date February 21, 1997
Days to Decision 86 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
41d faster than avg
Panel avg: 127d · This submission: 86d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EMA Cement, Dental
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3275
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 - EMA Cement, Dental

All 297
Devices cleared under the same product code (EMA) and FDA review panel - the closest regulatory comparables to K964773.
PULPDENT OX-OUT
K972445 · Pulpdent Corp. · Oct 1997
HI DENSE TC
K971927 · Shofu Dental Corp. · Jun 1997
SPETEMP
K964808 · Ultradent Products, Inc. · Feb 1997
SPETEMP EF
K964809 · Ultradent Products, Inc. · Jan 1997
PULPDENT ENDODONTIC POST CEMENT KIT
K962747 · Pulpdent Corp. · Sep 1996
STERI-OSS TEMPORARY IMPLANT CEMENT
K963078 · Steri-Oss, Inc. · Sep 1996