OSTEOTEC SILICONE FINGER IMPLANT
Apr 2015
417d
Osteotec, Ltd.
1
Total
1
Cleared
0
Denied
Osteotec, Ltd. — FDA 510(k) Submissions
Osteotec, Ltd. has submitted 1 FDA 510(k) premarket notifications since 2015, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Prosthesis, Finger, Constrained, Polymer . Use the specialty filter in the sidebar to narrow results.
1 devices