Syntheon LAA Exclusion System, Syntheon LAA Selection Guide
Oct 2022
268d
Syntheon
1
Total
1
Cleared
0
Denied
Syntheon — FDA 510(k) Submissions
Syntheon has submitted 1 FDA 510(k) premarket notifications since 2022, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Left Atrial Appendage Clip, Implantable . Use the specialty filter in the sidebar to narrow results.
1 devices