Cleared Traditional

K024250 - MATCH PRESS PRESSABLE CERAMIC

K024250 is an FDA 510(k) clearance for MATCH PRESS PRESSABLE CERAMIC, manufactured by Davis Schottlander & Davis, Ltd.. The device is a Class 2 Dental device with product code EIH cleared through the Traditional 510(k) pathway after a 245-day FDA review.

K024250 · Davis Schottlander & Davis, Ltd. · Dental device
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Aug 2003
Decision
245d
Days
Class 2
Risk

K024250 is an FDA 510(k) clearance for the MATCH PRESS PRESSABLE CERAMIC. Classified as Powder, Porcelain (product code EIH), Class II - Special Controls.

Submitted by Davis Schottlander & Davis, Ltd. (Tonawanda, US). The FDA issued a Cleared decision on August 25, 2003 after a review of 245 days - an extended review cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.6660 - 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 Davis Schottlander & Davis, Ltd. devices

FDA 510(k) Submission Details - K024250

510(k) Number K024250 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 23, 2002
Decision Date August 25, 2003
Days to Decision 245 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
118d slower than avg
Panel avg: 127d · This submission: 245d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

EIH Device Classification - Class 2, Special Controls

Product Code EIH Powder, Porcelain
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.6660
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 - EIH Powder, Porcelain

All 313
Devices cleared under the same product code (EIH) and FDA review panel - the closest regulatory comparables to K024250.
CARRARA PRESS SYSTEM
K033667 · Dentsply Intl. · Jan 2004
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K033553 · Dentsply Intl. · Dec 2003
VINTAGE AL
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KAVO EVEREST ZS-BLANK MODELS, 42, 20, AND 60
K032081 · Kavo America · Jul 2003
IMAGINE REFLEX
K031326 · Wieland Dental + Technik GmbH & Co. KG · Jun 2003
KAVO EVEREST G-BLANK, KAVO EVEREST G-CERAM, COATING CERAMIC LF-3-PFM, GLAZE AND COLORINGS/STAINING/SHADES
K030607 · Kavo America · May 2003