ATOZ Mini-Screw
Dec 2021
297d
Mk Meditech, Inc.
1
Total
1
Cleared
0
Denied
Mk Meditech, Inc. — FDA 510(k) Submissions
Mk Meditech, Inc. has submitted 1 FDA 510(k) premarket notifications since 2021, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Implant, Endosseous, Orthodontic . Use the specialty filter in the sidebar to narrow results.
1 devices