2 results
Approved WMOCompleted
The primary objective of the study is to demonstrate non-inferiority of the KineSpring System, when compared to standard HTO surgery in improving pain and function outcomes at 24 months in patients with primarily unicompartmental medial knee…
Approved WMOCompleted
The primary objective of this study is to assess the efficacy and safety of LifeSeal* Kit as measured by the change in overall anastomotic leak rates in subjects undergoing low anterior resection with an anastomosis below 10 cm from the anal verge,…