Medical Device Manufacturer · US , Sunnyvale , CA

Cormatrix Cardiovascular, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2005

Total

Cleared

Denied

Cormatrix Cardiovascular, Inc. has 7 FDA 510(k) cleared medical devices. Based in Sunnyvale, US.

Historical record: 7 cleared submissions from 2005 to 2018. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Cormatrix Cardiovascular, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Cormatrix Cardiovascular, Inc.

7 devices

1-7 of 7