Surgical Devices, A Global Business Unit Covidien - FDA 510(k) Cleare...
Recent clearances: COVIDIEN SPORTS SURGERY AS MENISCAL REPAIR DEVICE WITH HIGH STRENGTH SUTURE, EEA HEMORRHOID STAPLER & ACCESSORIES, COVIDIEN SPORTS SURGERY AS MENISCAL REPAIR DEVICE
3
Total
3
Cleared
0
Denied
FDA 510(k) Regulatory Record - Surgical Devices, A Global Business Unit Covidien General & Plastic Surgery ✕
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