Cleared Special

K213700 - MULTIX Impact

K213700 is the FDA 510(k) clearance for MULTIX Impact by Siemens Medical Solutions USA, Inc.. It is a Class 2 Radiology device (product code KPR) cleared through the Special 510(k) pathway after a 20-day FDA review.

K213700 · Siemens Medical Solutions USA, Inc. · Radiology device
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Dec 2021
Decision
20d
Days
Class 2
Risk

K213700 is an FDA 510(k) clearance for the MULTIX Impact, MULTIX Impact C. Classified as System, X-ray, Stationary (product code KPR), Class II - Special Controls.

Submitted by Siemens Medical Solutions USA, Inc. (Malvern, US). The FDA issued a Cleared decision on December 13, 2021 after a review of 20 days - a notably fast clearance cycle.

This device falls under the Radiology FDA review panel, regulated under 21 CFR 892.1680 - the FDA radiology and imaging software oversight framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Siemens Medical Solutions USA, Inc. devices

Submission Details

510(k) Number K213700 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 23, 2021
Decision Date December 13, 2021
Days to Decision 20 days
Submission Type Special
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
87d faster than avg
Panel avg: 107d · This submission: 20d
Pathway characteristics
Modification to existing cleared device.

Device Classification

Product Code KPR System, X-ray, Stationary
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 892.1680
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 - KPR System, X-ray, Stationary

All 164
Devices cleared under the same product code (KPR) and FDA review panel - the closest regulatory comparables to K213700.
ExamVue Duo
K213057 · Jpi Healthcare Co, Ltd. · Feb 2022
Straight Arm DDR
K214012 · Konica Minolta Healthcare Americas, Inc. · Jan 2022
Philips Radiology Smart Assistant
K212186 · Philips Medical Systems Dmc GmbH · Dec 2021
DigitalDiagnost
K210692 · Philips Medical Systems Dmc GmbH · Apr 2021
Proteus XR/f, Models ST and ET, Multirad and Multirad NET Radiographic Systems
K203537 · Sedecal., Sa. · Feb 2021
MULTIX Impact
K203345 · Siemens Medical Solutions USA, Inc. · Jan 2021