An Investigation of the Metal Concentration in Patients Implanted With the PRESTIGE LP™ Cervical Disc at Two Contiguous Levels in the Cervical Spine

Phase

TERMINATED

Status

Enrollment

INDUSTRY

Sponsor class

Stopped Study terminated prematurely as agreed by the FDA. The FDA were satisfied that no further data was required, despite the total number of patients who completed the study in full not being the agreed upon number.

Conditions

Cervical Degenerative Disc Disease
Radiculopathy
Myelopathy

Interventions

DEVICE: PRESTIGE LP™ Cervical Disc

Sponsor

Medtronic Spinal and Biologics