Cleared Traditional

K931996 - MODEL PDEXA BONE DENSITOMETER

K931996 is an FDA 510(k) clearance for MODEL PDEXA BONE DENSITOMETER, manufactured by Norland Corp.. The device is a Class 2 Radiology device with product code KGI cleared through the Traditional 510(k) pathway after a 649-day FDA review.

K931996 · Norland Corp. · Radiology device
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Feb 1995
Decision
649d
Days
Class 2
Risk

K931996 is an FDA 510(k) clearance for the MODEL PDEXA BONE DENSITOMETER. Classified as Densitometer, Bone (product code KGI), Class II - Special Controls.

Submitted by Norland Corp. (Fort Atkinson, US). The FDA issued a Cleared decision on February 1, 1995 after a review of 649 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1170 - 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: High-complexity regulatory submission. Elevated predicate reliance profile. The extended review timeline suggests the FDA required additional documentation before confirming substantial equivalence - a pattern common in complex or first-of-kind Radiology submissions.

View all Norland Corp. devices

FDA 510(k) Submission Details - K931996

510(k) Number K931996 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 23, 1993
Decision Date February 01, 1995
Days to Decision 649 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
542d slower than avg
Panel avg: 107d · This submission: 649d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

KGI Device Classification - Class 2, Special Controls

Product Code KGI Densitometer, Bone
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1170
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 - KGI Densitometer, Bone

All 70
Devices cleared under the same product code (KGI) and FDA review panel - the closest regulatory comparables to K931996.
BONE MINERAL DENSITOMETER
K941362 · Hologic, Inc. · Aug 1995
EXPERT MORPHOMERTY SOFTWARD
K950611 · Lunar Corp. · May 1995
LUNAR EXPERT
K945526 · Lunar Corp. · Apr 1995
HOLOGIC QDR-3000 X-RAY BONE DENSITOMETER
K943505 · Hologic, Inc. · Jan 1995
DTX-100
K926300 · Hologic, Inc. · Jul 1993
HOLOGIC QDR-2000 X-RAY BONE DENSITOMETER
K913321 · Hologic, Inc. · Nov 1991