# Depuy Acromed, Inc.

- Location (FDA's records): Raynham, MA
- FDA decisions: 1 (2001–2001): 1 510(k) clearance
- Product codes: KWQ (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 3 (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
- Depuy, Inc.: 1 (https://510kreport.com/company/depuy)
- Acromed Corp.: 1 (https://510kreport.com/company/acromed)
- Medtronic Sofamor Danek: 1 (https://510kreport.com/company/medtronic-sofamor-danek)

## Firms that cite its devices most
- Medos International SARL: 1 (https://510kreport.com/company/medos-international)
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)
- Paradigm Spine, LLC: 1 (https://510kreport.com/company/paradigm-spine)

## Its most-cited devices
- K012916: Frontier Anterior Scoliosis System (2001), cited by 3

## Recent decisions
- K012916: Frontier Anterior Scoliosis System (Nov 27, 2001)

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