FDA 510(k) Applications Submitted by Atrium Medical Corporation
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K231972 |
07/03/2023 |
Advanta VXT Vascular Graft, Flixene Vascular Graft |
Atrium Medical Corporation |
| K130142 |
01/22/2013 |
FLIXENE IFG VASCULAR GRAFT |
ATRIUM MEDICAL CORPORATION |
| K110110 |
01/14/2011 |
ATRIUM CENTRILFX MESH |
ATRIUM MEDICAL CORPORATION |
| K201305 |
05/15/2020 |
Auto transfusion (ATS) Chest Drains: Ocean Water Seal Chest Drain, Oasis Dry Suction Water Seal Chest Drain, Express Dry Seal Chest Drain |
Atrium Medical Corporation |
| K151386 |
05/26/2015 |
C-QUR, C-QUR FX, C-QUR TacShield, C-QUR V-Patch, C-QUR CentriFX, C-QUR Mosaic |
ATRIUM MEDICAL CORPORATION |
| K151437 |
05/29/2015 |
ProLite Mesh, ProLite Ultra Mesh, ProLoop Mesh Plug |
ATRIUM MEDICAL CORPORATION |
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