Depuy Mitek, Inc., A Johnson and Johnson Company is one of 13027 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Depuy Mitek, Inc., A Johnson and Johnson Company - FDA 510(k) Cleared...
Recent clearances: HEALIX ADVANCE KNOTLESS PEEK ANCHOR (6.5MM), ORTHOCORD, 6-8MM X 30 MM INTRAFIX PEEK TAPERED SCREW 7-9MM X 30MM INTRAFIX PEEK TAPERED SCREW 8-10MM X 30 MM INTRAFIX PEEK TAPERED
3
Total
3
Cleared
0
Denied
Depuy Mitek, Inc., A Johnson and Johnson Company has 3 FDA 510(k) cleared medical devices. Based in Raynham, US.
Historical record: 3 cleared submissions from 2012 to 2013. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Depuy Mitek, Inc., A Johnson and Johnson Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Depuy Mitek, Inc., A Johnson and Johnson Company
3 devices