Outcome of a Biocomposite Interference Screw/ ACL Surgery
ID Number 08-0311Principal Investigator(s)
Department(s) or Division(s)
This Clinical Outcomes Study is designed to evaluate post-procedure Computerized Tomography (CT’s) and Magnetic Resonance Imaging (MRI), to determine soft tissue and osteoconductive (bioreplaceable) activity at the site of implantation of the Milagro Interference Screw after the device has been used for reconstruction in standard ACL procedures. Continued safety of the Milagro device will also be tracked at the study assessment interval.
Recruiting Patients: Yes