# K171461: SkyPlate Detector for Philips Radiography/Fluoroscopy Systems

- Pathway: 510(k) (Traditional)
- Applicant: Philips Medical Systems Dmc GmbH
- Decided: Jul 7, 2017 after 50 days
- Product code: MQB (Solid State X-Ray Imager (Flat Panel/Digital Imager))
- Device class: 2
- Regulation: 21 CFR 892.1680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 9 generations back to K803130 (1981). 29 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 31 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K141736: Philips Prograde; Philips Eleva Workspot for Digital Diagnost, Philips Medical Systems Dmc GmbH (2014) Summary page 4.

## Most influential descendants
- K210985: 1717FCC (2021), 0 descendants of its own

## Indications for use
As a part of a radiographic system, the SkyPlate Detector for Philips Radiography/Fluoroscopy Systems is intended to acquire, process, store, display and export digital radiographic images. The SkyPlate Detector for Philips Radiography/Fluoroscopy Systems is suitable for all routine radiography exams, including specialist areas like intensive care, trauma, or pediatric work, excluding mammography.

Source page: https://510kreport.com/device/K171461
Methodology: https://510kreport.com/methodology