OsOpia Synthetic Bone Void Filler
Oct 2020
115d
Revisios BV
1
Total
1
Cleared
0
Denied
Revisios BV — FDA 510(k) Submissions
Revisios BV has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Bone Grafting Material, Synthetic . Use the specialty filter in the sidebar to narrow results.
1 devices