Cleared Traditional

K203345 - MULTIX Impact

K203345 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 Traditional 510(k) pathway after a 55-day FDA review.

K203345 · Siemens Medical Solutions USA, Inc. · Radiology device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jan 2021
Decision
55d
Days
Class 2
Risk

K203345 is an FDA 510(k) clearance for the MULTIX Impact. 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 January 7, 2021 after a review of 55 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. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.

View all Siemens Medical Solutions USA, Inc. devices

Submission Details

510(k) Number K203345 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 13, 2020
Decision Date January 07, 2021
Days to Decision 55 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
52d faster than avg
Panel avg: 107d · This submission: 55d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

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 K203345.
MULTIX Impact, MULTIX Impact C
K213700 · Siemens Medical Solutions USA, Inc. · 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 C
K203340 · Siemens Medical Solutions USA, Inc. · Jan 2021
Apolo D / Apolo S
K202388 · Vmi Tecnologias Ltda · Dec 2020
MiniCAT 2D
K201825 · Xoran Technologies, LLC · Nov 2020