# K914546: Angled Blade Plate

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: Nov 29, 1991 after 49 days
- Product code: KTW (Appliance, Fixation, Nail/Blade/Plate Combination, Single Component)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
10 later devices descend from it; 6 cite it directly.
0 of 11 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
- K112085: Synthes LCP Pediatric Plate Systems (2011), 4 descendants of its own
- K210247: OsteoCentric Integrated Hip Fastener System (2021), 1 descendant of its own
- K200246: JPS JuniOrtho Plating System (2020), 1 descendant of its own
- K080109: Synthes (Usa) Modular Blade Plate System (2008), 1 descendant of its own
- K221787: Auxein's DHS/DCS Plate System (2023), 0 descendants of its own

Source page: https://510kreport.com/device/K914546
Methodology: https://510kreport.com/methodology