Cleared Traditional

K903112 - PART NUMBER: TA-1118 TAP

K903112 is an FDA 510(k) clearance for PART NUMBER: TA-1118 TAP, manufactured by Minimatic Implant Technology. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 123-day FDA review.

K903112 · Minimatic Implant Technology · Dental device
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Nov 1990
Decision
123d
Days
Class 2
Risk

K903112 is an FDA 510(k) clearance for the PART NUMBER: TA-1118 TAP. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Minimatic Implant Technology (Deerfield Beach, US). The FDA issued a Cleared decision on November 13, 1990 after a review of 123 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3640 - 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 Minimatic Implant Technology devices

FDA 510(k) Submission Details - K903112

510(k) Number K903112 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received July 13, 1990
Decision Date November 13, 1990
Days to Decision 123 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
4d faster than avg
Panel avg: 127d · This submission: 123d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

DZE Device Classification - Class 2, Special Controls

Product Code DZE Implant, Endosseous, Root-form
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3640
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 - DZE Implant, Endosseous, Root-form

All 1291
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K903112.
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