# Depuy Synthes Spine

- Location (FDA's records): Raynham, MA
- FDA decisions: 3 (2014–2019): 3 510(k) clearances
- Names in FDA's records: Depuy Synthes Spine (2); Depuy Synthes Spine, Inc. (1)
- Product codes: MDI (1), MAX (1), MQP (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 1 (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.: 1 (https://510kreport.com/company/medtronic-sofamor-danek-usa)
- Medos Sarl: 1 (https://510kreport.com/company/medos)
- Synthes Spine: 1 (https://510kreport.com/company/synthes-spine)
- Synthes (USA) Products, LLC: 1 (https://510kreport.com/company/synthes-usa-products)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)

## Firms that cite its devices most
- OrthoPediatrics Corp.: 1 (https://510kreport.com/company/orthopediatrics)

## Its most-cited devices
- K142587: Vertical Expandable Prosthetic Titanium Rib (2014), cited by 1

## Recent decisions
- K183054: SYNMESH System (May 23, 2019)
- K181231: DePuy Synthes T-PAL Spacer System (Dec 6, 2018)
- K142587: Vertical Expandable Prosthetic Titanium Rib (Nov 18, 2014)

Source page: https://510kreport.com/company/depuy-synthes-spine