VCFix Spinal System
May 2025
88d
Amber Implants
1
Total
1
Cleared
0
Denied
Amber Implants — FDA 510(k) Submissions
Amber Implants has submitted 1 FDA 510(k) premarket notifications since 2025, 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