# Stryker Cmf

- Location (FDA's records): Kalamazoo, MI
- FDA decisions: 2 (2006–2007): 2 510(k) clearances
- Product codes: MQN (1), NEA (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
- Howmedica Corp.: 3 (https://510kreport.com/company/howmedica)
- Synthes (Usa): 2 (https://510kreport.com/company/synthes-usa)
- Howmedica Osteonics Corp.: 1 (https://510kreport.com/company/howmedica-osteonics)
- Stryker Corp.: 1 (https://510kreport.com/company/stryker)
- Stryker Instruments: 1 (https://510kreport.com/company/stryker-instruments)
- Walter Lorenz Surgical, Inc.: 1 (https://510kreport.com/company/walter-lorenz-surgical)

## Firms that cite its devices most
- KLS-Martin L.P.: 1 (https://510kreport.com/company/kls-martin)

## Its most-cited devices
- K071628: Stryker External Fixation System (2007), cited by 1

## Recent decisions
- K071628: Stryker External Fixation System (Aug 10, 2007)
- K060750: Stryker Injectable Cement (Apr 19, 2006)

Source page: https://510kreport.com/company/stryker-cmf