A?TOMIC? Nitinol Fixation System
Jan 2024
112d
Rmr Ortho, LLC
1
Total
1
Cleared
0
Denied
Rmr Ortho, LLC — FDA 510(k) Submissions
Rmr Ortho, LLC 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 Staple, Fixation, Bone . Use the specialty filter in the sidebar to narrow results.
1 devices