Synovis Life Technologies, Inc. (Baxter International Inc.) - FDA 510...
1
Total
1
Cleared
0
Denied
Synovis Life Technologies, Inc. (Baxter International Inc.) has 1 FDA 510(k) cleared medical devices. Based in St. Paul, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Synovis Life Technologies, Inc. (Baxter International Inc.) Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Synovis Life Technologies, Inc....
1 devices