# K002517: Uss Vas

- Pathway: 510(k) (Traditional)
- Applicant: Synthes (Usa)
- Decided: Sep 12, 2000 after 28 days
- Product code: KWP (Appliance, Fixation, Spinal Interlaminal)
- Device class: 2
- Regulation: 21 CFR 888.3050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
662 later devices descend from it; 3 cite it directly.
2 of 663 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
- K082572: Uss Iliosacral, Uss Polyaxial (2008), 659 descendants of its own
- K091445: CD Horizon Spinal System (2010), 581 descendants of its own
- K082914: Clampfix (2008), 350 descendants of its own
- K090605: Clampfix (2009), 349 descendants of its own
- K103287: Synthes 6.0 Cocr and CPT TI-3 Rods (2011), 348 descendants of its own

Source page: https://510kreport.com/device/K002517
Methodology: https://510kreport.com/methodology