# K153154: Asnis JFX System

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Trauma AG
- Decided: Dec 28, 2015 after 56 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
No predicates in its family tree.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K191289: Bone Screw Line Addition (2019), 2 descendants of its own
- K202817: GEO Bone Screw System (2020), 1 descendant of its own
- K230946: Accelerate Compression Screw System-Small Product Code ACC-S; Accelerate Compression Screw System-Medium Product Code ACC-M; Accelerate Compression Screw System-Large Product Code ACC-L (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K153154
Methodology: https://510kreport.com/methodology