The U.S. Department of Justice announced it would end its four year investigation related to off-label use of Medtronic's Infuse for spinal fusions.

AxioMed Spine Corp. has announced it has received the CE mark approval for its Freedom cervical disc, according to a news release.

The Food and Drug Administration granted 14 spine device-related clearances in April, according to an FDA report.

TranS1, a Wilmington, N.C.-based spine device company, reported a 26 percent decrease in revenue for the first quarter of 2012.

Here are 20 orthopedic and spine device company leadership moves so far this year.

The Food and Drug Administration granted 33 orthopedic- and spine-related device clearances in April.

Jupiter, Fla.-based company BioRestorative Therapies has announced improvements in the latest version of its stem cell disc delivery device, which is used for treating bulging and herniated discs.

Medtronic launched the POWEREASE System, a system of electronic instruments designed for use during instrumented spine surgery.

The Food and Drug Administration granted 17 spine-related medical device clearances in March.

Integra LifeSciences launched its Integra CUSA NXT Bone Tips for expanded application of the CURSA NXT Ultrasonic Tissue Ablation System.