# Stuart

- Location (FDA's records): Greensburg, PA
- FDA decisions: 5 (1982–1990): 5 510(k) clearances
- Product codes: KWQ (2), KWP (1), EZX (1), JDN (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K897141: Slot Staples and Adaptor for Zielke Spinal Fixatio (Jun 21, 1990)
- K890601: Stuart Titanium Surgical Mesh (Mar 16, 1989)
- K851414: Segmental Spinal Rods (Jun 28, 1985)
- K843445: Sacral Bar (Feb 13, 1985)
- K820034: Anterior Distraction System (Mar 11, 1982)

Source page: https://510kreport.com/company/stuart