Depuy Mitek, A Johnson & Johnson Company is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Depuy Mitek, A Johnson & Johnson Company - FDA 510(k) Cleared Devices
Recent clearances: Milagro / Milagro Advance Interference Screw, 4.5mm Healix Ti Anchor, with 2 or 3 strands of #2 Permacord suture, 5.5mm Healix Ti Anchor, with 2 or 3 strands of #2 Permacord suture, 6.5mm Healix Ti Anchor, with 2 or 3 strands of #2 Permacord suture,, VAPR ARCTIC SUCTION ELECTRODE
Depuy Mitek, A Johnson & Johnson Company has 58 FDA 510(k) cleared orthopedic devices. Based in Norwood, US.
Historical record: 58 cleared submissions from 2004 to 2015.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Depuy Mitek, A Johnson & Johnson Company
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