XD880A Ultrasonic Osteotomy Surgical System
Apr 2018
253d
Morley Research Consortium
1
Total
1
Cleared
0
Denied
Morley Research Consortium — FDA 510(k) Submissions
Morley Research Consortium has submitted 1 FDA 510(k) premarket notifications since 2018, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Instrument, Surgical, Sonic And Accessory/attachment . Use the specialty filter in the sidebar to narrow results.
1 devices