Odontoid Fracture Study Treated With Pulsed Electromagnetic Fields

Inclusion Criteria: * Subjects must be 50 years of age or older at the time of consent * Subject must have radiographic evidence (x-ray , MRI and CT scan) of a Type II odontoid fracture * Subject must have MRI evidence that the fracture occurred within 30 days of study enrollment * Subject must have VAS neck pain score of greater than 4 (\>4) * Subject must have radiographic evidence that the fracture is displaced ≤ 5 mm in any direction and/or have a fracture gap of ≤ 3 mm due to angulation * Subject must use a rigid cervical collar (Miami J, Philadelphia or Aspen) for a minimum of three months post-injury * Subject must have a DEXA scan within 6 months prior to enrollment (can be done within one week of baseline visit) * Subject must be willing and able to follow all study procedures and return for all study visits * Subject must be willing to sign an Informed Consent Document Exclusion Criteria: * Subject has undergone systematic administration, within 30 days prior to the fracture, of any type of corticosteroid, antineoplastic, immunostimulation or immunosuppressive agents * Subject is on chronic anticoagulation, or has a bleeding disorder * Subject is pregnant, nursing or plans to become pregnant during the study * Subject has a chronic Type II odontoid fracture that occurred more than 21 days prior to enrollment * Subject has a Type II odontoid fracture displaced \>5 mm * Subject has a mental or physical condition that would prevent him from complying with the study protocol, including the physician obtaining an accurate neurologic exam * Subject was recommended for surgery to treat the fracture but subject refused surgery * Subject is a prisoner * Subject has participated in another clinical trial within the last 90 days