Cleared Traditional

K163296 - SOMATOM go.Up

K163296 is the FDA 510(k) clearance for SOMATOM go.Up by Siemens Medical Solutions USA, Inc.. It is a Class 2 Radiology device (product code JAK) cleared through the Traditional 510(k) pathway after a 119-day FDA review.

K163296 · Siemens Medical Solutions USA, Inc. · Radiology device
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Mar 2017
Decision
119d
Days
Class 2
Risk

K163296 is an FDA 510(k) clearance for the SOMATOM go.Up, SOMATOM go.Now. Classified as System, X-ray, Tomography, Computed (product code JAK), Class II - Special Controls.

Submitted by Siemens Medical Solutions USA, Inc. (Malvern, US). The FDA issued a Cleared decision on March 21, 2017 after a review of 119 days - within the typical 510(k) review window.

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 Siemens Medical Solutions USA, Inc. devices

Submission Details

510(k) Number K163296 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 22, 2016
Decision Date March 21, 2017
Days to Decision 119 days
Submission Type Traditional
Review Panel Radiology (RA)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
12d slower than avg
Panel avg: 107d · This submission: 119d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

Device Classification

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 581
Devices cleared under the same product code (JAK) and FDA review panel - the closest regulatory comparables to K163296.
Philips iCT CT System
K162838 · Philips Medical Systems (Cleveland), Inc. · Apr 2017
IQon Spectral CT
K163711 · Philips Medical Systems (Cleveland), Inc. · Apr 2017
Scan&GO
K163297 · Siemens Medical Solutions USA, Inc. · Mar 2017
HITACHI Supria Whole-body X-ray CT System Phase 3
K163528 · Hitachi Medical Systems America, Inc. · Mar 2017
syngo. CT Neuro Perfusion
K163284 · Siemens Medical Solutions USA, Inc. · Mar 2017
syngo.CT Extended Functionality
K163341 · Siemens Medical Solutions USA, Inc. · Feb 2017