# Zimmer Knee Creations, Inc.

- Location (FDA's records): Exton, PA
- FDA decisions: 2 (2014–2019): 2 510(k) clearances
- Names in FDA's records: Zimmer Knee Creations, Inc. (1); Zimmer Knee Creations (1)
- Product codes: FMF (1), MQV (1)
- Predicates its devices cite: 7 (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
- Etex Corp.: 4 (https://510kreport.com/company/etex)
- Pinnacle Spine Group, LLC: 2 (https://510kreport.com/company/pinnacle-spine-group)
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)

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

## Its most-cited devices
- K133021: Mixing Syringe System (2014), cited by 1

## Recent decisions
- K190814: AccuFill Bone Substitute Material (Jun 10, 2019)
- K133021: Mixing Syringe System (Jan 13, 2014)

Source page: https://510kreport.com/company/zimmer-knee-creations