# Spinal Balance, Inc.

- Location (FDA's records): Toledo, OH
- FDA decisions: 2 (2015–2016): 2 510(k) clearances
- Product codes: NKB (2)
- Predicates its devices cite: 5 (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

## Firms whose devices it cites most
- Corelink, LLC: 1 (https://510kreport.com/company/corelink)
- Medtronic Sofamor Danek USA, Inc.: 1 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Stryker Spine: 1 (https://510kreport.com/company/stryker-spine)
- The Skeletal Design Partnership, Ltd.: 1 (https://510kreport.com/company/skeletal-design-partnership)

## Its most-cited devices
- K151770: Libra Pedicle Screw System (2015), cited by 1

## Recent decisions
- K162750: Libra Pedicle Screw System (Oct 27, 2016)
- K151770: Libra Pedicle Screw System (Nov 20, 2015)

Source page: https://510kreport.com/company/spinal-balance