V-STRUT? Vertebral Implant
Feb 2024
29d
Hyprevention
1
Total
1
Cleared
0
Denied
Hyprevention — FDA 510(k) Submissions
Hyprevention has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Cement, Bone, Vertebroplasty . Use the specialty filter in the sidebar to narrow results.
1 devices