# K925351: Synthes (U.S.a.) Anterior Spinal Plate

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: Nov 5, 1993 after 379 days
- Product code: KWQ (Appliance, Fixation, Spinal Intervertebral Body)
- Device class: 2
- Regulation: 21 CFR 888.3060
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
56 later devices descend from it; 2 cite it directly.
0 of 57 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
- K970048: Synthes (Usa)Titanium Locking Plate System (Tilps) (1997), 54 descendants of its own
- K010466: Tether Acfs (2001), 43 descendants of its own
- K121514: Anodyne Anterior Cervical Plate System (2012), 21 descendants of its own
- K163104: Terrace™ Anterior Cervical Plate System (2017), 18 descendants of its own
- K190016: Lateral Plate System (2019), 15 descendants of its own

Source page: https://510kreport.com/device/K925351
Methodology: https://510kreport.com/methodology