Cleared Traditional

K881890 - PROVISCEM OR PROVISCELL EUGENOL-FREE DENTAL CEMENT

K881890 is an FDA 510(k) clearance for PROVISCEM OR PROVISCELL EUGENOL-FREE DE..., manufactured by Specialites Septodont. The device is a Class 2 Dental device with product code EMA cleared through the Traditional 510(k) pathway after a 71-day FDA review.

K881890 · Specialites Septodont · Dental device
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Jul 1988
Decision
71d
Days
Class 2
Risk

K881890 is an FDA 510(k) clearance for the PROVISCEM OR PROVISCELL EUGENOL-FREE DENTAL CEMENT. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by Specialites Septodont (Washington, US). The FDA issued a Cleared decision on July 15, 1988 after a review of 71 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 Specialites Septodont devices

FDA 510(k) Submission Details - K881890

510(k) Number K881890 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received May 05, 1988
Decision Date July 15, 1988
Days to Decision 71 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
56d faster than avg
Panel avg: 127d · This submission: 71d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EMA Device Classification - Class 2, Special Controls

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 430
Devices cleared under the same product code (EMA) and FDA review panel - the closest regulatory comparables to K881890.
INTERIM, TEMPORARY CEMENT
K884081 · Scientific Pharmaceuticals, Inc. · Dec 1988
RESUBMITTED EMA DENTIN CEMENT
K883770 · G-C Intl. Corp. · Nov 1988
COE PAK AUTO MIX, REGULAR OR HARD SET
K881422 · Coe Laboratories, Inc. · Oct 1988
LIGHT-CURED ZIONOMER CEMENT
K881918 · Den-Mat Corp. · Jul 1988
IONOSCEM OR IONOSCELL GLASS IONOMER DENTAL CEMENT
K881661 · Specialites Septodont · Jun 1988
KERR XR BOND
K880250 · Kerr Corporation (Danbury) · Jun 1988