# K242096: dS FootAnkle Coil 8ch 1.5T

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems Nederland B.V.
- Decided: Aug 12, 2024 after 25 days
- Product code: MOS (Coil, Magnetic Resonance, Specialty)
- Device class: 2
- Regulation: 21 CFR 892.1000
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K050514 (2005). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050514: Models Fac-63 and Fac-127 Foot and Ankle Coils, Mri Devices Corporation (2005) Summary page 4.

## Indications for use
The dS FootAnkle Coil Sch 1.5T is intended to be used in conjunction with Philips Magnetic Resonance Scanner to produce diagnostic images of the foot and ankle that can be interpreted by a trained physician.

Source page: https://510kreport.com/device/K242096
Methodology: https://510kreport.com/methodology