Broomfield, Colo.-based spinal device company Lanx has introduced a website for patients with chronic leg and back pain.
Spinal Tech
Smith & Nephew has released an extension to the LEGION Total Knee System, featuring implants thinner in the medial and lateral dimension.
Zimmer issued an urgent recall of its PEEK Ardis Inserter, an instrument for implanting the PEEK Ardis Interbody Spacer in the spine.
Aurora Spine, a minimally invasive regenerative technologies company, recently announced the completion of the ISO stage one and two audits and is now certified by the British Standards Institute.
The FDA granted 510(k) clearance to Ascendx Spine for its VCF Repair System for vertebral compression fractures.
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San Jose, Calif.-based medical device company SI-BONE has a peer-reviewed journal article published on its iFuse Implant System.
Blue Belt Technologies' NavioPFS unicondylar knee replacement system has received FDA 510(k) clearance.
NuVasive has received Japanese clearance for its CoRoent Large Impacted and CoRoent Large Tapered titanium alloy spine implants.
Here are 12 orthopedic and spine device executive moves over the past few months.
Orthofix's investigation into its bone growth stimulation business has concluded, and the company will pay $43 million to fully resolve matters, both criminal and civil.