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Searching News Database:  Vitoss 

 HSMN NewsFeed - 12 Jun 2018
NuVasive Launches AttraX Scaffold Biologic And Reports First Clinical Use
Devices Orthopaedic Neurosurgery Product Launch
 HSMN NewsFeed - 23 May 2016
NuVasive Launches Next Generation Biologics Technology
Devices Orthopaedic Neurosurgery Product Launch
 HSMN NewsFeed - 16 May 2011
Orthovita, Inc. Agrees To Be Acquired by Stryker Corporation for $3.85 Per Share in Cash
Devices Mergers & Acquisitions
 HSMN NewsFeed - 11 Apr 2011
Orthovita Announces Presentation of Clinical Results Evaluating Vitagel(TM) Surgical Hemostat in Reducing Blood Loss During Primary Unilateral Total Knee Arthroplasty
Devices Orthopaedic Surgery
 HSMN NewsFeed - 16 Feb 2011
Orthovita Launches Vitoss(TM) Bioactive Foam-2X Bone Graft Substitute at AAOS (American Academy of Orthopedic Surgeons) Meeting
Devices Orthopaedic
 HSMN NewsFeed - 11 Feb 2011
Orthovita Receives FDA Clearance for Vitoss(TM) Bimodal Bone Graft Substitute
Devices Orthopaedic Regenerative Medicine FDA
 HSMN NewsFeed - 7 Dec 2010
Orthovita Receives FDA Clearance for Vitoss(TM) Bioactive Foam-2X Bone Graft Substitute
Devices Orthopaedic FDA
 HSMN NewsFeed - 6 Oct 2010
Orthovita Announces Presentation of Cortoss 24-Month Pivotal Study Results at the 25th Annual Meeting of the North American Spine Society
Devices Orthopaedic Neurosurgery
 HSMN NewsFeed - 4 Oct 2010
Orthovita Receives FDA Clearance for VITOMATRIX(TM) Bone Graft Substitute in Dental Applications
Devices Dental FDA
 HSMN NewsFeed - 1 Apr 2009
Orthovita Submits Additional Data to FDA in Support of Its 510(k) Application for the Use of CORTOSS Bone Augmentation Material in Vertebral Augmentation
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 22 Sep 2008
Orthovita Announces New VITOSS Bioactive Foam Pack Bone Graft Substitute
Devices Orthopaedic Neurosurgery
 HSMN NewsFeed - 14 Apr 2008
Orthovita Introduces VITASURE(TM) Absorbable Hemostat as Part of its Strategy to Leverage its Biomaterials Sales Organization
Devices Distribution
 HSMN NewsFeed - 15 Jan 2008
Orthovita Submits 510(k) Application to FDA for the Use of CORTOSS(R) Bone Augmentation Material in Vertebral Augmentation
Devices Orthopaedic Neurosurgery
 HSMN NewsFeed - 6 Aug 2007
Orthovita Receives CE Mark for VITAGEL(R) Surgical Hemostat and CELLPAKER(R) Plasma Collection System
Devices Regulatory
 HSMN NewsFeed - 21 Feb 2007
Orthovita Announces Completion of Patient Enrollment in Its U.S. Pivotal Clinical Study for the Use of CORTOSS(R) in the Treatment of Vertebral Compression Fractures
Devices Neurosurgery Orthopaedic
 HSMN NewsFeed - 7 Feb 2007
Orthovita Announces Appointment of Chief Business Officer and Chief Financial Officer
Devices Personnel
 HSMN NewsFeed - 5 Feb 2007
Orthovita Confirms That 510(k) Submission May Be Used to Seek Clearance for CORTOSS(R) Bone Augmentation Material for the Treatment of Vertebral Compression Fractures
Devices Orthopaedic Neurosurgery FDA
 HSMN NewsFeed - 22 Jan 2007
FDA Approves Orthovita's PMA Supplement for the CELLPAKER(R) Plasma Collection System Used in Conjunction with the VITAGEL(R) Surgical Hemostat
Devices FDA
 HSMN NewsFeed - 8 Nov 2006
Orthovita Enters into Binding Letter of Intent to Purchase the VITAGEL(TM) Profit-Sharing Royalty Rights From Angiotech Pharmaceuticals (US), Inc.
Devices Licensing
 HSMN NewsFeed - 9 Oct 2006
First U.S. Presentation of CORTOSS(R) IDE Pivotal Clinical Preliminary Data to Be Presented in a Poster at the Congress of Neurological Surgeons in Chicago
Devices Neurosurgery Orthopaedic
 HSMN NewsFeed - 14 Sep 2006
Orthovita Announces First Public Podium Presentation of CORTOSS(R) IDE Pivotal Clinical Data in the Treatment of Vertebral Compression Fractures at the European Society of Neuroradiology Meeting in Geneva
Devices Orthopaedic
 HSMN NewsFeed - 12 Sep 2006
Albert J. Pavucek, Jr. Joins Orthovita as Vice President Corporate Controller
Devices Personnel
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