Cleared Traditional

K913175 - MIRACLE MIX CAPS GLASS IONOMER CEMENT I...

K913175 is an FDA 510(k) clearance for MIRACLE MIX CAPS GLASS IONOMER CEMENT I..., manufactured by G-C Intl. Corp.. The device is a Class 2 Dental device with product code EJJ cleared through the Traditional 510(k) pathway after a 163-day FDA review.

K913175 · G-C Intl. Corp. · Dental device
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Dec 1991
Decision
163d
Days
Class 2
Risk

K913175 is an FDA 510(k) clearance for the MIRACLE MIX CAPS GLASS IONOMER CEMENT INCAPSULES. Classified as Alloy, Amalgam (product code EJJ), Class II - Special Controls.

Submitted by G-C Intl. Corp. (Scottsdale, US). The FDA issued a Cleared decision on December 27, 1991 after a review of 163 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3070 - 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 G-C Intl. Corp. devices

FDA 510(k) Submission Details - K913175

510(k) Number K913175 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 17, 1991
Decision Date December 27, 1991
Days to Decision 163 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
36d slower than avg
Panel avg: 127d · This submission: 163d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EJJ Device Classification - Class 2, Special Controls

Product Code EJJ Alloy, Amalgam
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3070
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 - EJJ Alloy, Amalgam

All 33
Devices cleared under the same product code (EJJ) and FDA review panel - the closest regulatory comparables to K913175.
TYTIN ADMIX
K951511 · Kerr Corporation (Danbury) · May 1995
SYBRALOY
K940675 · Sybron Dental Specialties, Inc. · Apr 1994
TYTIN
K935535 · Kerr Corporation (Danbury) · Mar 1994
DW 236
K905204 · Ivoclar North America, Inc. · Mar 1991
DW 235
K905205 · Ivoclar North America, Inc. · Dec 1990
ARTALLOY (POWDER)
K902247 · Degussa AG · Jul 1990