Cleared Traditional

K102677 - BODYTOM NL 4000

K102677 is an FDA 510(k) clearance for BODYTOM NL 4000, manufactured by Neurologica Corporation. The device is a Class 2 Radiology device with product code JAK cleared through the Traditional 510(k) pathway after a 190-day FDA review.

K102677 · Neurologica Corporation · Radiology device
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Mar 2011
Decision
190d
Days
Class 2
Risk

K102677 is an FDA 510(k) clearance for the BODYTOM NL 4000. Classified as System, X-ray, Tomography, Computed (product code JAK), Class II - Special Controls.

Submitted by Neurologica Corporation (Danvers, US). The FDA issued a Cleared decision on March 24, 2011 after a review of 190 days - an extended review cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1750 - 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 Neurologica Corporation devices

FDA 510(k) Submission Details - K102677

510(k) Number K102677 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 15, 2010
Decision Date March 24, 2011
Days to Decision 190 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review Yes - reviewed by an FDA-accredited third party
Regulatory Context
Review time vs. panel average
83d slower than avg
Panel avg: 107d · This submission: 190d
Pathway characteristics
Predicate-based equivalence. No clinical trials required. Third-party reviewed.

JAK Device Classification - Class 2, Special Controls

Product Code JAK System, X-ray, Tomography, Computed
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1750
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 - JAK System, X-ray, Tomography, Computed

All 640
Devices cleared under the same product code (JAK) and FDA review panel - the closest regulatory comparables to K102677.
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K101888 · Hitachi Medical Systems America, Inc. · Apr 2011
COMPUTED TOMOGRAPHY X-RAY SYSTEM
K102102 · VATECH Co., Ltd. · Mar 2011
SOMATOM DEFINITION AS
K103127 · Siemens Medical Solutions USA, Inc. · Mar 2011
DENTAL COMPUTED TOMOGRAPHY X-RAY SYSTEM
K102259 · VATECH Co., Ltd. · Feb 2011