Cleared Traditional

K163317 - ELECTROmatic

K163317 is an FDA 510(k) clearance for ELECTROmatic, manufactured by Kaltenbach & Voigt Gmgh. The device is a Class 1 Dental device with product code EBW cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K163317 · Kaltenbach & Voigt Gmgh · Dental device
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Feb 2017
Decision
90d
Days
Class 1
Risk

K163317 is an FDA 510(k) clearance for the ELECTROmatic. Classified as Controller, Foot, Handpiece And Cord (product code EBW), Class I - General Controls.

Submitted by Kaltenbach & Voigt Gmgh (Biberach, DE). The FDA issued a Cleared decision on February 21, 2017 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Dental FDA review panel, regulated under 21 CFR 872.4200 - 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 Kaltenbach & Voigt Gmgh devices

FDA 510(k) Submission Details - K163317

510(k) Number K163317 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 23, 2016
Decision Date February 21, 2017
Days to Decision 90 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
37d faster than avg
Panel avg: 127d · This submission: 90d
Pathway characteristics
Predicate-based equivalence.

EBW Device Classification - Class 1, General Controls

Product Code EBW Controller, Foot, Handpiece And Cord
Device Class Class 1 - General Controls
CFR Regulation 21 CFR 872.4200
What this classification means

Class I devices are subject to general controls only and most are exempt from 510(k) premarket notification. They represent the lowest regulatory burden in the FDA device framework.

Regulatory Peers - EBW Controller, Foot, Handpiece And Cord

All 33
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