DEPUY SYNTHES INJECTABLE POLYMER SYSTEM (IPS)
Mar 2015
304d
Depuy Synthes Companies of Johnson & Johnson
1
Total
1
Cleared
0
Denied
Depuy Synthes Companies of Johnson & Johnson — FDA 510(k) Submissions
Depuy Synthes Companies of Johnson & Johnson 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 Fastener, Plate, Cranioplasty . Use the specialty filter in the sidebar to narrow results.
1 devices