Medical Device Manufacturer · US , Bozeman , MT

Jotec GmbH - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2003

1

Total

1

Cleared

0

Denied

FDA 510(k) Regulatory Record - Jotec GmbH Cardiovascular ✕

1 devices

1-1 of 1

Cleared Jan 24, 2003

FLOWLINE BIOPORE EPTFE VASCULAR GRAFT

Cardiovascular · 259d