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Spineway sets up the governing structure for its US subsidiary

November 15, 2018 / Source: SPINEWAY Spineway, specialist in surgical implants and instruments for treating disorders of the spinal column (spine), is reorganizing and setting up the governing structure for its US subsidiary with the arrival of a new CEO. Pursuant to the strategic plan, Stéphane Le Roux, CEO of Spineway SA, launched the reorganization of the

By |2018-11-15T21:52:25+00:00November 15th, 2018|Spine|

NuVasive Launches First-Of-Its-Kind Brigade® Lateral Implant And Instrumentation Optimized For Lateral Anterior Lumbar Interbody Fusion Spine Surgery

SAN DIEGO, Nov. 15, 2018 /PRNewswire/ -- NuVasive, Inc. (NASDAQ: NUVA), the leader in spine technology innovation, focused on transforming spine surgery with minimally disruptive, procedurally integrated solutions, today announced the U.S. commercial launch of Brigade® Lateral, the industry's first interbody implant and instrumentation optimized for lateral anterior lumbar interbody fusion (ALIF) spine surgery. NuVasive's Lateral ALIF™ is a

By |2018-11-15T21:32:28+00:00November 15th, 2018|Spine, Top Stories|

OSN Interview with David Derminio – Executive Vice President Commercialization at Myoscience

Dave, would you please give us a brief overview of your Orthopedic career and how you got started in the business? Immediately following my graduation from the Business School at Arizona State University I went to work for American Hospital Supply Corporation. As I progressed through my career with AHSC, they provided excellent training in

By |2018-11-15T18:00:15+00:00November 15th, 2018|Recon|

Simplify Medical Completes Enrollment in U.S. IDE Pivotal Trial of Simplify® Disc for Two-Level Cervical Disc Replacement

SUNNYVALE, Calif., Nov. 14, 2018 (GLOBE NEWSWIRE) -- Simplify Medical Pty Ltd., maker of the Simplify® cervical artificial disc, today announced that it has completed the enrollment and treatment of all patients in its U.S. Investigational Device Exemption (IDE) pivotal trial evaluating the Simplify® Disc for two-level cervical disc replacement. The Simplify Disc is designed for biomechanical

By |2018-11-15T17:21:26+00:00November 15th, 2018|Spine|

Xtant Medical Announces Third Quarter 2018 Financial Results

BELGRADE, MT, Nov. 14, 2018 (GLOBE NEWSWIRE) -- Xtant Medical Holdings, Inc. (NYSE American: XTNT), a leader in the development of regenerative medicine products and medical devices, today reported financial and operating results for the third quarter ended September 30, 2018. Third Quarter 2018 Financial Highlights and Recent Announcements: Revenue for the third quarter of

By |2018-11-15T16:50:15+00:00November 15th, 2018|Financial|

Nanovis Expands the Range of Footprints for its Signature FortiCore Posterior Lumbar Interbody Fusion System

CARMEL, IND. (PRWEB) NOVEMBER 14, 2018 Nanovis, a leader in nanomedicine for the spine, today announced adding 22mm and 25mm lengths to its FortiCore® rotatable Posterior Lumbar Interbody Fusion (PLIF) devices. With over 5,000 FortiCore interbodies now implanted, Nanovis plans to further accelerate its technology driven growth with the expansion of their FortiCore PLIF product line

By |2018-11-15T16:37:37+00:00November 15th, 2018|Spine, Top Stories|

Camber Spine Announces First Surgeries With ENZA®-A Titanium ALIF

KING OF PRUSSIA, Pa., Nov. 14, 2018 /PRNewswire/ -- Camber Spine, a leading innovator in spine and medical technologies, today announced the completion of 45 successful implantations utilizing ENZA®-A Titanium ALIF in less than 30 days since it's launch. Seth Anderson, Vice President of Sales and Surgeon relations commented "We are extremely pleased with the feedback we are receiving

By |2018-11-14T22:42:32+00:00November 14th, 2018|Spine|

Spokane Doctor Advancing Performance of Total Knee Replacements

SPOKANE, Wash., Nov. 13, 2018 /PRNewswire/ -- Dr. David F. Scott, a leading orthopedic surgeon and researcher, is exploring new, innovative knee implant designs and surgical techniques made for custom fit total knee replacements. The basis for this improved knee replacement performance is an anatomical approach, whereby an implant is placed in the native joint line of a patient's

By |2018-11-14T18:14:28+00:00November 14th, 2018|Recon|

Bio2 Technologies, Inc. Receives FDA IDE Approval to Begin Clinical Study of Resorbable Cervical Interbody Device for Spinal Fusion

WOBURN, Mass., Nov. 13, 2018 /PRNewswire/ -- Bio2 Technologies, Inc., a privately held orthopedics company, announced today that it received U.S. Food and Drug Administration ("FDA") approval to begin enrollment in an IDE clinical study to evaluate Vitrium as a cervical interbody fusion device.  Vitrium will be evaluated as a structural device that facilitates bone remodeling via a

By |2018-11-14T17:15:56+00:00November 14th, 2018|Regulatory|

Managing Partner of KICVentures and Former J.P. Morgan Analyst Predicts Continued Valuation Growth in the Spine Device Market

BOSTON (PRWEB) NOVEMBER 13, 2018 Aditya Humad, Managing Partner of KICVentures, released an analysis of the spine technology market last week that asserts it is still trending upward with growing valuations based on a largely under-served and expanding global patient population. Humad’s analysis describes market consolidation, pricing pressure and increased competition as reasons often cited by institutional

By |2018-11-14T16:35:55+00:00November 14th, 2018|Spine|