Cleared Traditional

K880250 - KERR XR BOND

K880250 is the FDA 510(k) clearance for KERR XR BOND by Kerr Corporation (Danbury). It is a Class 2 Dental device (product code EMA) cleared through the Traditional 510(k) pathway after a 133-day FDA review.

K880250 · Kerr Corporation (Danbury) · Dental device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jun 1988
Decision
133d
Days
Class 2
Risk

K880250 is an FDA 510(k) clearance for the KERR XR BOND. Classified as Cement, Dental (product code EMA), Class II - Special Controls.

Submitted by Kerr Corporation (Danbury) (Washington, US). The FDA issued a Cleared decision on June 1, 1988 after a review of 133 days - within the typical 510(k) review window.

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: 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 Kerr Corporation (Danbury) devices

Submission Details

510(k) Number K880250 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received January 20, 1988
Decision Date June 01, 1988
Days to Decision 133 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
6d slower than avg
Panel avg: 127d · This submission: 133d
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 284
Devices cleared under the same product code (EMA) and FDA review panel - the closest regulatory comparables to K880250.
TEMP BOND NE
K894219 · Kerr Corporation (Danbury) · Sep 1989
CHELON-FIL
K884475 · Espe GmbH (Us) · Dec 1988
INTERIM, TEMPORARY CEMENT
K884081 · Scientific Pharmaceuticals, Inc. · Dec 1988
KERR XR IONOMER
K880251 · Kerr Corporation (Danbury) · Jun 1988
PORCELITE DUAL CURE CEMENT
K880685 · Kerr Corporation (Danbury) · May 1988
KETAC-BOND APLICAP
K874788 · Espe GmbH (Us) · Apr 1988