Cleared Traditional

K040757 - SIC PRO

K040757 is an FDA 510(k) clearance for SIC PRO, manufactured by Sic Invent AG. The device is a Class 2 Dental device with product code DZE cleared through the Traditional 510(k) pathway after a 384-day FDA review.

K040757 · Sic Invent AG · Dental device
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Apr 2005
Decision
384d
Days
Class 2
Risk

K040757 is an FDA 510(k) clearance for the SIC PRO. Classified as Implant, Endosseous, Root-form (product code DZE), Class II - Special Controls.

Submitted by Sic Invent AG (Basel, CH). The FDA issued a Cleared decision on April 13, 2005 after a review of 384 days - an unusually long review period, suggesting complex equivalence evaluation.

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. Elevated predicate reliance profile. 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 Sic Invent AG devices

FDA 510(k) Submission Details - K040757

510(k) Number K040757 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 25, 2004
Decision Date April 13, 2005
Days to Decision 384 days
Submission Type Traditional
Review Panel Dental (DE)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
257d slower than avg
Panel avg: 127d · This submission: 384d
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 797
Devices cleared under the same product code (DZE) and FDA review panel - the closest regulatory comparables to K040757.
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