# K792291: Synthes Reconstructive Plates 'Y' Plates

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: Dec 6, 1979 after 23 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.
80 later devices descend from it; 7 cite it directly.
0 of 81 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
- K960533: K3 Bone Screw System (1996), 61 descendants of its own
- K960537: K2 Bone Screw System (1996), 41 descendants of its own
- K120493: Mini Cannulated Headed and Headless Screw Set (2012), 39 descendants of its own
- K123890: Acumed Cannulated Screw System (2013), 36 descendants of its own
- K190586: Monster® Screw System (2019), 21 descendants of its own

Source page: https://510kreport.com/device/K792291
Methodology: https://510kreport.com/methodology