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HSMN NewsFeed - 8 May 2023
HAPPE Spine Announces FDA Clearance for the INTEGRATE-C(TM) Interbody Fusion System
HAPPE Spine Announces FDA Clearance for the INTEGRATE-C(TM) Interbody Fusion System
HSMN NewsFeed - 24 Sep 2021
Intelivation Technologies Launches Advantage-C(TM) PEEK Cervical Interbody Fusion Device
Intelivation Technologies Launches Advantage-C(TM) PEEK Cervical Interbody Fusion Device
HSMN NewsFeed - 22 Sep 2021
Kleiner Device Labs Receives FDA Market Clearance for KG2 Surge Flow-Thru Interbody System
Kleiner Device Labs Receives FDA Market Clearance for KG2 Surge Flow-Thru Interbody System
HSMN NewsFeed - 18 Nov 2020
NuVasive Expands Proprietary Porous PEEK Portfolio with Cohere XLIF Interbody
NuVasive Expands Proprietary Porous PEEK Portfolio with Cohere XLIF Interbody
HSMN NewsFeed - 11 Apr 2019
Nuvasive Advances Lateral Single-Position Surgery With Introduction Of X360(TM) System At AANS 2019
Nuvasive Advances Lateral Single-Position Surgery With Introduction Of X360(TM) System At AANS 2019
HSMN NewsFeed - 19 Mar 2019
Centinel Spine Appoints Dirk M. Kuyper and Gregory Rainey to its Board of Directors
Centinel Spine Appoints Dirk M. Kuyper and Gregory Rainey to its Board of Directors
HSMN NewsFeed - 10 Oct 2018
SpineEX(R) Announces FDA Clearance of Sagittae(R) Lateral Lumbar Interbody Fusion Devices
SpineEX(R) Announces FDA Clearance of Sagittae(R) Lateral Lumbar Interbody Fusion Devices
HSMN NewsFeed - 7 Jun 2018
Centinel Spine Announces 510(k) Clearance of FLX(TM) Platform of 3D Printed All-Titanium Interbodies
Centinel Spine Announces 510(k) Clearance of FLX(TM) Platform of 3D Printed All-Titanium Interbodies
HSMN NewsFeed - 4 Jan 2018
NuVasive Extends First-Of-Its-Kind Porous PEEK Interbody To TLIF And PLIF Procedures
NuVasive Extends First-Of-Its-Kind Porous PEEK Interbody To TLIF And PLIF Procedures
HSMN NewsFeed - 13 Jun 2017
Vertera Spine Receives New CMS ICD-10 Code for Radiolucent Porous Interbody Fusion Devices
Vertera Spine Receives New CMS ICD-10 Code for Radiolucent Porous Interbody Fusion Devices
HSMN NewsFeed - 24 May 2016
Interventional Spine, Inc. announces FDA Clearance of Lordotic Opticage(TM)
Interventional Spine, Inc. announces FDA Clearance of Lordotic Opticage(TM)
HSMN NewsFeed - 25 Jan 2016
Amedica Enhances Valeo II(TM) Product Family With the Addition of Its Second Generation Cervical System
Amedica Enhances Valeo II(TM) Product Family With the Addition of Its Second Generation Cervical System
HSMN NewsFeed - 10 Nov 2015
Interventional Spine Gains FDA Clearance of Advanced Design of Its Expandable Opticage(R) for Spinal Fusion
Interventional Spine Gains FDA Clearance of Advanced Design of Its Expandable Opticage(R) for Spinal Fusion
HSMN NewsFeed - 15 Oct 2015
Nanovis Launches Expanded FortiCore Line of Interbody Fusion Devices at NASS
Nanovis Launches Expanded FortiCore Line of Interbody Fusion Devices at NASS
HSMN NewsFeed - 6 Oct 2015
Vertera Spine Announces FDA Clearance of the First Surface Porous PEEK Interbody Fusion Device
Vertera Spine Announces FDA Clearance of the First Surface Porous PEEK Interbody Fusion Device
HSMN NewsFeed - 18 Aug 2015
Aurora Spine Receives CE Mark Approval for Sterile-Packed TiNano(R) Coated Interbody Systems
Aurora Spine Receives CE Mark Approval for Sterile-Packed TiNano(R) Coated Interbody Systems
HSMN NewsFeed - 12 Nov 2014
Globus Medical Announces ALTERA(TM) Minimally Invasive Articulating Expandable Spacer
Globus Medical Announces ALTERA(TM) Minimally Invasive Articulating Expandable Spacer
HSMN NewsFeed - 14 Jul 2014
Titan Spine Receives FDA Clearance to Launch Endoskeleton(R) TL Device for Lateral Spinal Fusion
Titan Spine Receives FDA Clearance to Launch Endoskeleton(R) TL Device for Lateral Spinal Fusion
HSMN NewsFeed - 9 Oct 2013
Tyber Medical Receives 510 (k) Clearance For TyPEEK(TM) And PEEK Interbody Systems
Tyber Medical Receives 510 (k) Clearance For TyPEEK(TM) And PEEK Interbody Systems
HSMN NewsFeed - 28 May 2013
Lanx Announces Initial Launch of TIMBERLINE(TM) MPF Lateral Modular Plate Fixation System
Lanx Announces Initial Launch of TIMBERLINE(TM) MPF Lateral Modular Plate Fixation System
HSMN NewsFeed - 27 Sep 2012
Amedica Receives FDA 510(k) Clearance For A Second Generation Interbody Fusion Device System
Amedica Receives FDA 510(k) Clearance For A Second Generation Interbody Fusion Device System
HSMN NewsFeed - 5 Apr 2011
Titan Spine Receives CE Mark Certification for Endoskeleton(R) Lumbar Interbody Fusion Devices
Titan Spine Receives CE Mark Certification for Endoskeleton(R) Lumbar Interbody Fusion Devices
HSMN NewsFeed - 18 Feb 2011
Zimmer Spine Introduces Industry's First Porous Metal Cervical Interbody Device
Zimmer Spine Introduces Industry's First Porous Metal Cervical Interbody Device
HSMN NewsFeed - 6 Oct 2010
DiFUSION Technologies Receives 510(k) Clearance of Xiphos(TM) Interbody Implants for Spinal Fusion
DiFUSION Technologies Receives 510(k) Clearance of Xiphos(TM) Interbody Implants for Spinal Fusion
HSMN NewsFeed - 18 Aug 2010
Aesculap Implant Systems, Inc. Receives FDA 510(k) Clearance for the A-Fix (SIBD) Spinal System
Aesculap Implant Systems, Inc. Receives FDA 510(k) Clearance for the A-Fix (SIBD) Spinal System
HSMN NewsFeed - 9 Nov 2009
Titan Spine Appoints Accomplished Spine Surgeon Paul Slosar, MD as Medical Director
Titan Spine Appoints Accomplished Spine Surgeon Paul Slosar, MD as Medical Director
HSMN NewsFeed - 12 Oct 2009
RSB Spine, LLC, Announces FDA Clearance for the InterPlate(R) C-Ti as an Anterior Cervical Plate
RSB Spine, LLC, Announces FDA Clearance for the InterPlate(R) C-Ti as an Anterior Cervical Plate
HSMN NewsFeed - 25 Mar 2009
Spinal Elements, Inc. and Paradigm BioDevices, Inc. Form Strategic Alliance
Spinal Elements, Inc. and Paradigm BioDevices, Inc. Form Strategic Alliance
HSMN NewsFeed - 18 Mar 2008
Titan Spine's ENDOSKELETON(R) TA Passes Test In Competitive Lower Back Pain Market
Titan Spine's ENDOSKELETON(R) TA Passes Test In Competitive Lower Back Pain Market
HSMN NewsFeed - 20 Jul 2007
Premier's Spine Implant Portfolio Produces $30 Million in Member Savings During First Year
Premier's Spine Implant Portfolio Produces $30 Million in Member Savings During First Year
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Interbody Fusion Device
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Interbody Fusion Device
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