Cleared Traditional

K895267 - ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT

K895267 is an FDA 510(k) clearance for ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT, manufactured by Artech Corp.. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 230-day FDA review.

K895267 · Artech Corp. · Dental device
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Apr 1990
Decision
230d
Days
Class 2
Risk

K895267 is an FDA 510(k) clearance for the ARTECH TYPE SS-HA SUBMERGED SCREW IMPLANT. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Artech Corp. (Chantilly, US). The FDA issued a Cleared decision on April 10, 1990 after a review of 230 days - an extended review cycle.

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 Artech Corp. devices

FDA 510(k) Submission Details - K895267

510(k) Number K895267 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received August 23, 1989
Decision Date April 10, 1990
Days to Decision 230 days
Submission Type Traditional
Review Panel Dental (DE)
Summary -
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
103d slower than avg
Panel avg: 127d · This submission: 230d
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 1324
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K895267.
CORE-VENT ARMENTARIUM
K900177 · Core-Vent Corp. · Jun 1990
INTEGRAL PLUS BIOINTEGRATED DENTAL IMPLANT SYSTEM
K900549 · Calcitek, Inc. · Jun 1990
O-RING PROSTHETIC ATTACHMENT DEVICE
K900545 · Calcitek, Inc. · Jun 1990
BONEFIT HOLLOW CYLINDER IMPLANTS
K894593 · Institut Straumann AG · Feb 1990
BONEFIT HOLLOW SCREW IMPLANTS
K894594 · Institut Straumann AG · Feb 1990
BONEFIT R SCREW IMPLANTS
K894595 · Institut Straumann AG · Feb 1990