Cleared Traditional

K961434 - VITA ZETA CROWN AND BRIDGE ACRYLIC VENE...

K961434 is the FDA 510(k) clearance for VITA ZETA CROWN AND BRIDGE ACRYLIC VENE... by Vident. It is a Class 2 Dental device (product code EBF) cleared through the Traditional 510(k) pathway after a 84-day FDA review.

K961434 · Vident · Dental device
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Jul 1996
Decision
84d
Days
Class 2
Risk

K961434 is an FDA 510(k) clearance for the VITA ZETA CROWN AND BRIDGE ACRYLIC VENEERING SYSTEM. Classified as Material, Tooth Shade, Resin (product code EBF), Class II - Special Controls.

Submitted by Vident (Brea, US). The FDA issued a Cleared decision on July 8, 1996 after a review of 84 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3690 - 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 Vident devices

Submission Details

510(k) Number K961434 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 15, 1996
Decision Date July 08, 1996
Days to Decision 84 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
43d faster than avg
Panel avg: 127d · This submission: 84d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code EBF Material, Tooth Shade, Resin
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3690
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 - EBF Material, Tooth Shade, Resin

All 584
Devices cleared under the same product code (EBF) and FDA review panel - the closest regulatory comparables to K961434.
PULPDENT DESENSITIZER
K963652 · Pulpdent Corp. · Oct 1996
TEAM ETCH
K963311 · Centrix, Inc. · Oct 1996
TARGIS SYSTEM
K962878 · Ivoclar North America, Inc. · Sep 1996
CENTRIX FLOFIL/CENTRIX FLOFIL WITH FLUORIDE
K960667 · Wallace A. Erickson & Co. · Jul 1996
KOLOR +
K961284 · Sybron Dental Specialties, Inc. · May 1996
ALPHA-DENT COMPOSITE SURFACE SEALANT
K960165 · Wallace A. Erickson & Co. · Mar 1996