Depuy Mitek, A Johnson and Johnson Company is one of 13040 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Depuy Mitek, A Johnson and Johnson Company - FDA 510(k) Cleared Devic...
Recent clearances: Healix BR Anchor, Healix PEEK Anchor, Healix Transtend, Gryphon T and P BR Anchor, Gryphon PEEK Anchor, VersaLok Anchor, Bioknotless BR Anchor, Lupine BR Anchor, PanaLok Anchor,PanaLok Anchor with Orthocord, PanaLok RC QuickAnchor Plus, GRYPHON BR ANCHOR W/PROKNOT TECHNOLOGY,GRYPHON PEEK ANCHOR W/ PROKNOT TECHNOLOGY, RIGIDLOOP ADJUSTABLE CORTICAL IMPLANT: STANDARD, LONG AND XL
3
Total
3
Cleared
0
Denied
Depuy Mitek, A Johnson and Johnson Company has 3 FDA 510(k) cleared medical devices. Based in Raynham, US.
Historical record: 3 cleared submissions from 2014 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Depuy Mitek, A Johnson and Johnson Company Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Depuy Mitek, A Johnson and Johnson Company
3 devices
Cleared
Oct 06, 2015
Healix BR Anchor, Healix PEEK Anchor, Healix Transtend, Gryphon T and P BR...
Orthopedic
249d
Cleared
Jul 08, 2014
GRYPHON BR ANCHOR W/PROKNOT TECHNOLOGY,GRYPHON PEEK ANCHOR W/ PROKNOT TECHNOLOGY
Orthopedic
118d
Cleared
Jul 07, 2014
RIGIDLOOP ADJUSTABLE CORTICAL IMPLANT: STANDARD, LONG AND XL
Orthopedic
147d