Atrium Medical Corporation - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Atrium Medical Corporation has 6 FDA 510(k) cleared medical devices. Based in Hudson, US.
Latest FDA clearance: Mar 2024. Active since 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Atrium Medical Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Atrium Medical Corporation
6 devices
Cleared
Mar 28, 2024
Advanta VXT Vascular Graft, Flixene Vascular Graft
Cardiovascular
269d
Cleared
Sep 03, 2021
Auto transfusion (ATS) Chest Drains: Ocean Water Seal Chest Drain, Oasis Dry...
Cardiovascular
476d
Cleared
Oct 22, 2015
C-QUR, C-QUR FX, C-QUR TacShield, C-QUR V-Patch, C-QUR CentriFX, C-QUR Mosaic
General & Plastic Surgery
149d
Cleared
Aug 27, 2015
ProLite Mesh, ProLite Ultra Mesh, ProLoop Mesh Plug
General & Plastic Surgery
90d
Cleared
Mar 15, 2013
FLIXENE IFG VASCULAR GRAFT
Cardiovascular
52d
Cleared
Feb 15, 2011
ATRIUM CENTRILFX MESH
General & Plastic Surgery
32d