Spinal Tech

The FDA cleared 12 spine devices in June.

The FDA cleared 21 orthopedic devices in June, including many for lower-extremity and spinal procedures.

Jason Toy, MD, of Austin-based Orthopedic Associates of Central Texas, debuted a new lateral interbody system made of 3D-printed titanium.

Centene has created a positive coverage policy for minimally invasive sacroiliac joint fusion, according to a July 14 news release.

From FDA clearances to strengthened partnerships, here are seven updates from spine and orthopedic device companies in the last week:

The FDA has granted breakthrough device designation for Spino Modulation's MIScoli system, a vertebral body tethering system to treat adolescent idiopathic scoliosis.

The FDA cleared Stryker's InSpace balloon implant for arthroscopic treatment of rotator cuff tears, the company said July 13.

Orthopedic devicemakers' general payments to surgeons plunged in 2020 compared to 2019 as elective surgeries and in-person visits were largely stunted because of the COVID-19 pandemic.

Medacta will pay at least $12 million to settle allegations of patent infringement and tortious interference against a developer of hip and knee implants.

Toronto-based device company Titan Medical named Stephen Lemieux CFO, according to a July 12 release.