interbody
-
Regulatory
MEDICREA® Announces FDA Clearance of the World’s First Patient-Matched Spinal Interbody Cages
February 11, 2020 LYON, France & NEW YORK–(BUSINESS WIRE)–MEDICREA® (Euronext Growth Paris : FR0004178572 – ALMED, PEA-PME eligible and OTCQX :…
Read More » -
Regulatory
DiFusion Inc. Announces FDA 510K Clearance for Xiphos™ ZFUZE™
November 04, 2019 AUSTIN, Texas–(BUSINESS WIRE)–DiFusion, Inc. today announced the FDA 510K clearance for the Xiphos-ZF Spinal interbody device. Xiphos-ZF…
Read More » -
Spine
Nexxt Spine Increases NEXXT MATRIXX® Offerings with Lordotic TLIF Oblique
August 28, 2019- Noblesville, IN- Nexxt Spine LLC, a pioneer in the design and manufacturing of innovative spinal solutions, is…
Read More » -
Spine
Interbody-Fusion Outcomes May Be Improved by Use of Invibio’s PEEK-OPTIMA™ HA Enhanced Polymer
THORNTON CLEVELEYS, UK (PRWEB) JANUARY 17, 2017 Early clinical results presented by surgeons at the 2016 annual meeting of the…
Read More » -
Hospitals
Medicrea Announces 510(k) Submission for FDA Clearance of Proprietary 3D-Printed Titanium Spinal Interbody Devices
January 09, 2017 01:30 AM Eastern Standard Time LYON, France & NEW YORK–(BUSINESS WIRE)–The Medicrea Group (Alternext Paris: FR0004178572 –…
Read More »