# Spartek Medical, Inc.

- Location (FDA's records): Alameda, CA
- FDA decisions: 2 (2010–2011): 2 510(k) clearances
- Product codes: NKB (2)
- Predicates its devices cite: 1 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Its most-cited devices
- K094002: Spartek Variable Angle Pedicle Screw Posterior Fusion System (2010), cited by 1

## Recent decisions
- K103383: Spartek Variable Angle Pedicle Screw Posterior Fusion System (Feb 17, 2011)
- K094002: Spartek Variable Angle Pedicle Screw Posterior Fusion System (May 7, 2010)

Source page: https://510kreport.com/company/spartek-medical