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Searching News Database:  autogenous bone graft 

 HSMN NewsFeed - 10 Jun 2022
Zavation Medical Products, LLC, receives FDA 510K Clearance for eZspand(TM) Lateral Cage as an addition to its eZspand(TM) Interbody System.
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 4 Jun 2018
Camber Spine Announces 510(k) Approval Of ENZA(TM)-A Titanium ALIF
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 25 Oct 2017
Zimmer Biomet Announces U.S. Launch of Vitality(R)+ and Vital(TM) Spinal Fixation Systems
Devices Neurosurgery Orthopaedic Product Launch
 HSMN NewsFeed - 7 Sep 2017
Spinal Resources, Inc.'s Swedge Pedicle Screw System Receives FDA 510(k) Clearance
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 24 May 2016
Interventional Spine, Inc. announces FDA Clearance of Lordotic Opticage(TM)
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 13 Nov 2014
Integra LifeSciences Announces FDA Clearance and Controlled Market Release of Expandable Interbody System for Spinal Surgery
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 12 Nov 2014
Globus Medical Announces ALTERA(TM) Minimally Invasive Articulating Expandable Spacer
Devices Orthopaedic Neurosurgery Product Launch
 HSMN NewsFeed - 25 Sep 2012
Precision Spine(TM) Announces FDA 510(k) Clearance for ReForm(TM) Pedicle Screw System
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 26 Jun 2012
Zimmer Introduces First Porous Metal Interbody Implant for Lumbar Spine in the United States
Devices Orthopaedic Neurosurgery
 HSMN NewsFeed - 28 Oct 2011
Spinal USA Gets FDA Approval for Two New Spinal Treatment Products
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 18 Feb 2011
Zimmer Spine Introduces Industry's First Porous Metal Cervical Interbody Device
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 18 Dec 2009
Medtronic Introduces the SOVEREIGN Spinal System for Lumbar Surgery
Devices Orthopaedic Neurosurgery
 HSMN NewsFeed - 19 Sep 2008
Scient'x Launches Tribeca(TM) TLIF Cage System
Devices Neurosurgery Orthopaedic
 HSMN NewsFeed - 29 Apr 2008
Medtronic Receives Approval to Market Smaller Kit Sizes of INFUSE(R) Bone Graft
Devices Orthopaedic FDA
 HSMN NewsFeed - 13 Dec 2007
BioMimetic Therapeutics Reports Positive Clinical Results for GEM OS(R)1 in Canadian Foot and Ankle Fusion Study
Devices Orthopaedic
 HSMN NewsFeed - 13 Jul 2007
BioMimetic Therapeutics' Clinical Investigator Presents Positive Interim Data on U.S. and Canadian Foot and Ankle Clinical Trials
Devices Orthopaedic
 HSMN NewsFeed - 13 Mar 2007
Medtronic Receives Approval to Market INFUSE Bone Graft for Certain Oral Maxillofacial and Dental Regenerative Applications
Devices Orthopaedic FDA
 HSMN NewsFeed - 13 Dec 2006
BioMimetic Therapeutics Announces Positive Results Using GEM OS1(TM) Bone Graft in Foot/Ankle Fusions
Devices Orthopaedic
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