The Food and Drug Administration granted 11 spine-related device 510(k) clearances in September, according to an FDA report.
The Latest
Researchers are now looking at ways to slow or reverse disc degeneration by administering growth factors to promote new extracellular matrix synthesis, according to a study published in Spine.
A recent article published in the European Spine Journal shows support for the use of orthopedic imaging company EOS's full body imaging system, according to an EOS news release.
Lanx, a Broomfield, Colo.-based spine device company, has formed the Surgeon Advisory Board, which will be chaired by Andrew Cappuccino, MD, of Buffalo Spine Surgery in Lockport, N.Y., according to a Lanx news release.
Spineology, a St. Paul, Minn.-based spine device company, has received FDA clearance for its Rampart line of interbody fusion implants, according to a Spineology news release.
A researcher in the department of engineering at the New Jersey Institute of Technology recently studied and presented his findings on treating patients with spinal cord injuries with micro-electrical stimulators, according to an NJIT news release.
Presbyterian Orthopaedic Hospital in Charlotte, N.C., part of Charlotte-based Presbyterian Healthcare, has submitted a certificate of need to build a replacement hospital at a cost of approximately $84 million, according to a health system news release.
Here are 15 executive changes among orthopedic and spine device companies over the past two months.
Starting today, Florida physicians can now look up patients on the statewide prescription drug database, according to a My Fox Orlando report.
Kentucky is beginning a pilot project with Ohio to prevent prescription drug abuse by sharing electronic prescribing data, according to a Courier-Journal report.
