Cleared Traditional

K972276 - CEREC 2 CROWN SOFTWARE

K972276 is an FDA 510(k) clearance for CEREC 2 CROWN SOFTWARE, manufactured by Siemens AG. The device is a Class 2 Dental device with product code ELW cleared through the Traditional 510(k) pathway after a 58-day FDA review.

K972276 · Siemens AG · Dental device
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Aug 1997
Decision
58d
Days
Class 2
Risk

K972276 is an FDA 510(k) clearance for the CEREC 2 CROWN SOFTWARE. Classified as Material, Impression (product code ELW), Class II - Special Controls.

Submitted by Siemens AG (North Attleboro, US). The FDA issued a Cleared decision on August 15, 1997 after a review of 58 days - a notably fast clearance cycle.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.3660 - 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 Siemens AG devices

FDA 510(k) Submission Details - K972276

510(k) Number K972276 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 18, 1997
Decision Date August 15, 1997
Days to Decision 58 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
69d faster than avg
Panel avg: 127d · This submission: 58d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

ELW Device Classification - Class 2, Special Controls

Product Code ELW Material, Impression
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.3660
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 - ELW Material, Impression

All 238
Devices cleared under the same product code (ELW) and FDA review panel - the closest regulatory comparables to K972276.
AQUASIL XLV SMART WETTING IMPRESSION MATERIAL
K973782 · Dentsply Intl. · Dec 1997
PROVIL NOVO
K973694 · Heraeus Kulzer, Inc. · Nov 1997
HYDROFLEX
K973343 · GC America, Inc. · Oct 1997
ELITE H-D VINYL POLYSILOXANE IMPRESSION MATERIALS .PUTTY SOFT/NORMAL SETTING /PUTTY SOFT/FAST SETTING
K972239 · Zhermack S.P.A. · Aug 1997
ELITE H-D HYDROPHILIC VINYL POLYSILOXANE IMPRESSION MATERIALS (LIGHT BODY/NORMAL,LIGHT BODY/FAST SETTING,REGULAR BODY,)
K972027 · Zhermack S.P.A. · Jul 1997
MEMOREG
K971155 · Heraeus Kulzer, Inc. · May 1997