# The Skeletal Design Partnership, Ltd.

- Location (FDA's records): Chesterland, OH
- FDA decisions: 1 (2012–2012): 1 510(k) clearance
- Product codes: NKB (1)
- Predicates its devices cite: 9 (0 its own); citations of its devices by later devices: 1 (0 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
- Medtronic Sofamor Danek USA, Inc.: 2 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Depuy Spine, Inc.: 2 (https://510kreport.com/company/depuy-spine)
- Depuyacromed: 2 (https://510kreport.com/company/depuyacromed)
- Acromed Corp.: 1 (https://510kreport.com/company/acromed)
- Buckman Co., Inc.: 1 (https://510kreport.com/company/buckman)
- Cross Medical Products, Inc.: 1 (https://510kreport.com/company/cross-medical-products)

## Firms that cite its devices most
- Spinal Balance, Inc.: 1 (https://510kreport.com/company/spinal-balance)

## Its most-cited devices
- K120074: Foundation Spinal System (2012), cited by 1

## Recent decisions
- K120074: Foundation Spinal System (Mar 14, 2012)

Source page: https://510kreport.com/company/skeletal-design-partnership