# K170040: BePOD Cannulated Arthrodesis Screws

- Pathway: 510(k) (Traditional)
- Applicant: Fournitures Hospitalieres Industrie
- Decided: Apr 4, 2017 after 89 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K000684 (2000). 41 ancestors in all.
No later device cites it as a predicate yet.
0 of 42 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K070617: Cannulated Screw, Fournitures Hospitalieres Industrie (2007) Summary page 5.
- K132217: Arthrex Compression FT Screws, Arthrex, Inc. (2013) Summary page 5.

## Indications for use
Arthrodesis cannulated screws are designed for the following indication: Arthrodesis of the metatarsal-phalangeal joint of the big toe.

Source page: https://510kreport.com/device/K170040
Methodology: https://510kreport.com/methodology