# K170418: Stryker SonicPin System

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Trauma GmbH
- Decided: Jun 20, 2017 after 127 days
- Product code: HTY (Pin, Fixation, Smooth)
- 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: 3 generations back to K050749 (2005). 4 ancestors in all.
No later device cites it as a predicate yet.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143063: Stryker SonicPin System, Stryker SonicAnchor System, Stryker Trauma GmbH (2015) Summary page 4.

## Indications for use
The Stryker SonicPin System is intended to maintain alignment and fixation of bone fractures, osteotomies or bone grafts in hallux valgus applications in the presence of appropriate immobilization (e.g. rigid fixation implants, cast and brace). The Stryker SonicPin is designed only to be inserted with the SonicFusion equipment.

Source page: https://510kreport.com/device/K170418
Methodology: https://510kreport.com/methodology