# Depuy Motech Acromed

- Location (FDA's records): Cleveland, OH
- FDA decisions: 4 (1998–1999): 4 510(k) clearances
- Product codes: MNI (2), MQP (1), KWQ (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 35 (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
- Acromed Corp.: 2 (https://510kreport.com/company/acromed)
- Orthopedic Equipment Co., Inc.: 1 (https://510kreport.com/company/orthopedic-equipment)

## Firms that cite its devices most
- Depuyacromed: 4 (https://510kreport.com/company/depuyacromed)
- Medos International SARL: 4 (https://510kreport.com/company/medos-international)
- Theken Surgical,Llc: 2 (https://510kreport.com/company/theken-surgical)
- Aesculap, Inc.: 2 (https://510kreport.com/company/aesculap)
- Spinal Edge, LLC: 2 (https://510kreport.com/company/spinal-edge)
- Depuy Spine, Inc.: 2 (https://510kreport.com/company/depuy-spine)
- Custom Spine, Inc.: 2 (https://510kreport.com/company/custom-spine)
- Sanacor: 1 (https://510kreport.com/company/sanacor)

## Its most-cited devices
- K990148: Stackable Cage System (1999), cited by 21
- K982443: Doc Ventral Cervical Stabilization System (1998), cited by 7
- K984350: VSP System (1999), cited by 6
- K984348: Timx Low Back System (1999), cited by 1

## Recent decisions
- K990148: Stackable Cage System (Sep 3, 1999)
- K984350: VSP System (Jan 20, 1999)
- K984348: Timx Low Back System (Jan 20, 1999)
- K982443: Doc Ventral Cervical Stabilization System (Jul 29, 1998)

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