Cleared Traditional

K103689 - PLANMECA PROMAX 3D MID

K103689 is the FDA 510(k) clearance for PLANMECA PROMAX 3D MID by Planmeca Oy. It is a Class 2 Radiology device (product code MUH) cleared through the Traditional 510(k) pathway after a 90-day FDA review.

K103689 · Planmeca Oy · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Mar 2011
Decision
90d
Days
Class 2
Risk

K103689 is an FDA 510(k) clearance for the PLANMECA PROMAX 3D MID. Classified as System, X-ray, Extraoral Source, Digital (product code MUH), Class II - Special Controls.

Submitted by Planmeca Oy (Helsinki, FI). The FDA issued a Cleared decision on March 17, 2011 after a review of 90 days - within the typical 510(k) review window.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 872.1800 - the FDA radiology and imaging software oversight 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 Radiology review framework, consistent with the majority of Class II 510(k) submissions.

View all Planmeca Oy devices

Submission Details

510(k) Number K103689 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received December 17, 2010
Decision Date March 17, 2011
Days to Decision 90 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
17d faster than avg
Panel avg: 107d · This submission: 90d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

Product Code MUH System, X-ray, Extraoral Source, Digital
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 872.1800
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 Radiology devices follow this clearance model.

Regulatory Peers - MUH System, X-ray, Extraoral Source, Digital

All 72
Devices cleared under the same product code (MUH) and FDA review panel - the closest regulatory comparables to K103689.
PCH-2500 DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM PAX-I DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM
K122155 · VATECH Co., Ltd. · Sep 2012
PCH-2500 DIGITAL EXTRAORAL SOURCE X-RAY SYSTEM
K113672 · VATECH Co., Ltd. · Mar 2012
CS 7600
K111649 · Carestream Health, Inc. · Sep 2011
DENTAL COMPUTED TOMOGRAPHY X-RAY SYSTEM
K102124 · VATECH Co., Ltd. · Oct 2010
DIGITAL X-RAY IMAGING SYSTEM (PAX-PRIMO) MODEL PAX-PRIMO
K100317 · VATECH Co., Ltd. · Mar 2010
XIOS PLUS WALL-MODULE
K081903 · Sirona Dental Systems GmbH · Aug 2008