Surgical Devices, A Global Business Unit Covidien - FDA 510(k) Cleare...
3
Total
3
Cleared
0
Denied
Surgical Devices, A Global Business Unit Covidien has 3 FDA 510(k) cleared medical devices. Based in North Haven, US.
Historical record: 3 cleared submissions from 2008 to 2009. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Surgical Devices, A Global Business Unit Covidien Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Surgical Devices, A Global Business...
3 devices
Cleared
May 04, 2009
COVIDIEN SPORTS SURGERY AS MENISCAL REPAIR DEVICE WITH HIGH STRENGTH SUTURE
General & Plastic Surgery
25d
Cleared
Feb 04, 2009
EEA HEMORRHOID STAPLER & ACCESSORIES
General & Plastic Surgery
47d
Cleared
Dec 01, 2008
COVIDIEN SPORTS SURGERY AS MENISCAL REPAIR DEVICE
General & Plastic Surgery
90d