Quarter Results/Regulatory Approval Kuros reports Corporate Highlights as of Q1 2024 including increase in direct MagnetOsTM sales 24-Apr-2024 / 07:00 CET/CEST Release of an ad hoc announcement ...

3D Systems has received 510 (k) clearance from the US Food and Drug Administration (FDA) for its VSP PEEK Cranial Implant.

The first anterior cervical interbody techniques were introduced by Cloward, and Robinson and Smith in the 1950s. Cloward's procedure involved insertion of a dowel graft following decompression.

As spine surgery technology and practice operations evolve, there are some trends that are ready to be sunsetted.

WEB Medical this week announced it received regulatory clearance for its Anterior Spine Truss System with Anchor Fixation.

Locate Bio, a pioneering orthobiologics company, today announces the successful completion of an oversubscribed £9.2 million funding round from both new investors and existing investors, Mercia ...

LIFEHAB is a randomized controlled trial in Norway comparing lumbar interbody fusion surgery with multidisciplinary rehabilitationNorway is a single-payer national health insurance systemLIFEHAB is ...

Background We compared the perioperative results and complications associated with PLIF and TLIF, and collected evidence for choosing the better fusion method. Methods A literature survey of the ...

NOT FOR DISTRIBUTION IN THE UNITED STATES OR OVER UNITED STATES WIRE SERVICES CARLSBAD, Calif., April 29, 2024 (GLOBE NEWSWIRE) -- (“Aurora Spine” or the “Company”) (TSXV: ASG) (OTCQB: ASAPF), a ...

Kuros announced 510(k) clearance from the U.S. Food and Drug Administration (FDA) for interbody use with MagnetOs Putty.* This significant milestone marks the fourth product from Kuros to receive ...