# K120363: Syngo RT Interface

- Pathway: 510(k) (Traditional)
- Applicant: Siemens Medical Solutions USA, Inc.
- Decided: Mar 20, 2012 after 43 days
- Product code: MUJ (System, Planning, Radiation Therapy Treatment)
- Device class: 2
- Regulation: 21 CFR 892.5050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K913770 (1991). 166 ancestors in all.
No later device cites it as a predicate yet.
0 of 167 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101119: Syngo Dosimetrist Workspace V2.7 Model: 1056864, Siemens Medical Solutions USA, Inc. (2010) Summary page 1.
- K093621: Syngo.Pet&CT Oncology, Siemens Medical Solutions USA, Inc. (2010) Summary page 1.
- K092519: Syngo.X, Siemens AG Medical Solutions (2009) Summary page 1.

## Indications for use
The syngo® RT Interface isas an accessory to the linear accelerator system to provide input to the planning for the delivery of x-ray photon and electron radiation for the therapeutic treatment of cancer where indicated. The syngo® RT Interface supports the oncology workflow as a medical application for viewing, manipulation, contouring, 3D visualization and comparison of medical images from multiple imaging modalities. This application allows the user to convert, store and export volume of interest (VOI) structures in DICOM® RT format for use in radiation therapy planning.

Source page: https://510kreport.com/device/K120363
Methodology: https://510kreport.com/methodology