# Zimmer Cas

- Location (FDA's records): Montreal, CA
- FDA decisions: 3 (2011–2014): 3 510(k) clearances
- Product codes: OLO (2), KWS (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 4 (0 its own)
- Recalls linked to its devices: 2 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Materialise NV: 2 (https://510kreport.com/company/materialise)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)
- Cleveland Clinic: 1 (https://510kreport.com/company/cleveland-clinic)
- Orthosoft, Inc.: 1 (https://510kreport.com/company/orthosoft)

## Firms that cite its devices most
- Pixee Medical: 1 (https://510kreport.com/company/pixee-medical)
- Tornier, Inc.: 1 (https://510kreport.com/company/tornier)
- Zimmer, Inc.: 1 (https://510kreport.com/company/zimmer)
- Orthosoft Inc (D/B/A Zimmer Cas): 1 (https://510kreport.com/company/orthosoft-d-b-a-zimmer-cas)

## Its most-cited devices
- K131129: Cas Psi Shoulder (2013), cited by 2
- K141601: Iassist Knee System (2014), cited by 1
- K110054: Navitrack System - OS Knee Universal, Cas Same Incision Tibia Reference (2011), cited by 1

## Recent decisions
- K141601: Iassist Knee System (Sep 11, 2014)
- K131129: Cas Psi Shoulder (Aug 20, 2013)
- K110054: Navitrack System - OS Knee Universal, Cas Same Incision Tibia Reference (Mar 24, 2011)

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