K2M Group Holdings, Inc., a global leader of complex spine and minimally invasive solutions focused on achieving three-dimensional Total Body Balance ™, today announced that it received a CE Mark for ...

AUSTIN, Texas--(BUSINESS WIRE)--LDR, a privately held medical device company offering innovative spinal implants for both non-fusion and fusion applications, announced that it has received 510(k) ...

MEMPHIS, TENN. - October 21, 2014 - Medtronic, Inc. (MDT) announced the U.S. launch of the DIVERGENCE(TM) Anterior Cervical Fusion System for the treatment of single-level cervical disc disease today ...

LDR Holding Corporation recently announced its ROI-C Cervical Cage has received FDA clearance to expand the indications of the device to include use with allograft. Previously, the device was cleared ...

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, ...

Renovis Surgical Technologies, Inc. today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market the Tesera™ SC – Porous Titanium Cervical Interbody ...

(MENAFN- PR Newswire) GENEVA, May 28, 2024 /PRNewswire/ -- Spineart, a fast-growing company specialized in spine surgery, proudly announces the 510(k) clearance from the U.S. Food and Drug ...

ST. LOUIS--(BUSINESS WIRE)--CoreLink, LLC, a leading designer and manufacturer of spinal implant systems, today announced the commercial launch and 510(k) clearance from the U.S. Food and Drug ...

We were unable to process your request. Please try again later. If you continue to have this issue please contact [email protected]. Back to Healio NuVasive Inc. announced it received FDA ...

Photos of highly activated bone forming cells at 14 days in culture, and electron microscopy showing the macroscopic, microscopic and nanometer scales features that in combination lead to maturing ...