Please provide your email address to receive an email when new articles are posted on . Cervical degenerative disc disease occurs when the functional spinal unit breaks down. It can lead to disabling ...

LAFAYETTE, Calif.--(BUSINESS WIRE)--Providence Medical Technology, Inc., an innovator in tissue-sparing cervical spine technology, today introduced its proprietary Cavux™ surface technology, designed ...

GENEVA, June 5, 2025 /PRNewswire/ -- Spineart announces the full-market launch of its SCARLET® AC-Ti secured anterior cervical cage in the United States. Following 510(k) clearance in May 2024, ...

Stryker Corp. has picked up a nod from the FDA to market the Tritanium C anterior cervical cage, an interbody fusion technology intended for use in the cervical spine. With this clearance, the ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com. Implanet has announced FDA 510(k) clearance of its ...

DUBLIN--(BUSINESS WIRE)--The "Interbody Fusion Cage Market by Product Type, Surgery, and End User : Global Opportunity Analysis and Industry Forecast, 2021-2030" report has been added to ...

), a leading medical device company focused on transforming spine surgery with minimally disruptive, procedurally-integrated solutions, announced today the first ever FDA 510(k) clearance of a ...

SAN DIEGO, March 29, 2017 /PRNewswire/ -- NuVasive, Inc. (NASDAQ: NUVA), a leading medical device company focused on transforming spine surgery with minimally disruptive, procedurally-integrated ...

FLOWOOD, Miss., July 17, 2018 /PRNewswire/ -- Zavation, an employee-owned medical device company that designs, develops, manufactures and distributes medical device products, announced today that it ...

Spinal device specialist NuVasive recently received section 501(k) FDA clearance for its X-Core Mini Cervical Expandable VBR System, a titanium vertebral-body replacement device used in the cervical ...