Barrigel Injectable Gel
May 2022
83d
Palette Life Sciences
1
Total
1
Cleared
0
Denied
Palette Life Sciences — FDA 510(k) Submissions
Palette Life Sciences 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 Hydrogel Spacer . Use the specialty filter in the sidebar to narrow results.
1 devices