# Depuy Motech

- Location (FDA's records): Warsaw, IN
- FDA decisions: 2 (1995–1995): 2 510(k) clearances
- Product codes: MNH (2)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 17 (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 that cite its devices most
- Stryker Spine: 7 (https://510kreport.com/company/stryker-spine)
- Stryker Corp.: 2 (https://510kreport.com/company/stryker)
- Spinecraft, LLC: 2 (https://510kreport.com/company/spinecraft)
- Corelink, LLC: 1 (https://510kreport.com/company/corelink)
- Life Spine, Inc.: 1 (https://510kreport.com/company/life-spine)
- Kalitec Direct, LLC: 1 (https://510kreport.com/company/kalitec-direct)
- Medos International SARL: 1 (https://510kreport.com/company/medos-international)
- Depuy, Inc.: 1 (https://510kreport.com/company/depuy)

## Its most-cited devices
- K950697: Depuy Motech Moss Miami Spinal System - Pedicle Fixation (1995), cited by 16
- K950695: Depuy Motech Moss Spinal System - Pedicle Fixation (1995), cited by 1

## Recent decisions
- K950695: Depuy Motech Moss Spinal System - Pedicle Fixation (Jul 21, 1995)
- K950697: Depuy Motech Moss Miami Spinal System - Pedicle Fixation (Jun 22, 1995)

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