Spine Procedures, Practices and News
May 10, 2013
Globus Medical, based in Audubon, Pa., has launched the FORTIFY I, an expandable corpectomy spacer with integrated screws for further stability in addition to supplemental fixation.
The Food and Drug Administration granted 19 510(k) clearances in April.
April 08, 2013
The Food and Drug Administration issued 13 spine-related device clearances in March.
February 14, 2013
Here are five recent financial reports from spine device companies or the spine business lines from orthopedics-focused device companies.
January 24, 2013
The implantable medical device market in the United States is expected to grow annually by 8 percent over seven years, according to Med City News.
December 20, 2012
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.
December 17, 2012
The Food and Drug Administration granted 16 spine-related clearances in November.
December 11, 2012
The Food and Drug Administration granted 36 orthopedic- and spine-related device clearances in November.
November 27, 2012
LDR was founded in France in 2000 and came to the United States in 2005. The company's strategy focused on a few areas of novel treatments to build success in the U.S. market. The company has been very successful with the ROI-C, ROI-A and Avenue L products which incorporate VerteBRIDGE Plating Technology, and looks forward to launching the Mobi-C cervical disc in the United States as well. Mobi-C is available in Europe, Asia and Latin America, and has just received conditional approval from the Food and Drug Administration for two-level disc replacement.