Medical Device Manufacturer · CA , Montreal

Orthosoft D/B/A Zimmer Cas - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2021

Total

Cleared

Denied

Orthosoft D/B/A Zimmer Cas has 7 FDA 510(k) cleared medical devices. Based in Montreal, CA.

Last cleared in 2023. Active since 2021. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Orthosoft D/B/A Zimmer Cas Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Orthosoft D/B/A Zimmer Cas

7 devices

1-7 of 7