2634 results found.
NuVasive Announces New CEO
NuVasive named J. Christopher Barry to succeed Gregory T. Lucier as Chief Executive Officer, effective next month. Mr. Lucier wil...
DePuy Synthes Reports 3Q18 Revenue, -4.2% vs. 3Q17
DePuy Synthes’ 3Q18 orthopaedic performance remains challenged with revenue of US $2,111.3MM, -4.2% vs. 3Q17.
Contract Manufacturer M&A: 2017-3Q18
Merger and acquisition activity is shaping the broader orthopaedic supply chain base, with contract manufacturers of all sizes transforming in the last decade to keep pace with their scaling device company customers. We've identified three M&A trends in this portion of the market—ones that ...
SYNOSTE Raises Funds for Smart Skeletal Deformity Correction Tools
SYNOSTE raised €5.1MM (~USD $5.9MM) to support the development of third-generation bone lengthening and deformation...
VISEON Gains FDA Clearance for Voyant Surgical Platform
Viseon received FDA 510(k) clearance to market the Voyant System for Minimally Invasive Spine Surgery access, visualizati...
SeaSpine Prices $50MM Public Offering of Stock
SeaSpine closed its underwritten public offering of 3,250,000 shares of its common stock for US $15.50/share, for gross proceeds of ~$50.4MM.
K2M Expands MESA Platform with FDA Clearance for Sagittal Imbalance Application
K2M received additional FDA 510(k) clearance for the MESA® Spinal System, supporting use of sagittal plane correction in idiopathic...
SpineEX Gains FDA Clearance for Sagittae LLIF
SpineEX received FDA 510(k) clearance to market its Sagittae® expandable device for minimally invasive lateral lumbar in...
NuVasive Awarded Neuromonitoring Services Contract with Premier
NuVasive Clinical Services was awarded a three-year, sole source supplier contract for Intraoperative Neuromonitoring
NuVasive Enters Partnership with Biedermann Technologies
NuVasive entered into a strategic partnership with Biedermann Technologies to integrate proprietary screw techno...
Safe Orthopaedics Posts 3Q18 Revenue Growth of 20%
Safe Orthopaedics posted 3Q18 revenue of €0.8MM (~US $0.9MM), +20% vs. 3Q17, with YTD18 revenue of €2.4MM (~$2.8M), +7...
NASS Conversations Reaffirm Spine’s Focus on Additive, Computer-Assisted, Materials
By Carolyn LaWell Speaking with device companies, suppliers and surgeons at the North American Spine Society Annual Meeting (NASS) confirmed our previous thoughts on the health of the spine market and the technologies driving its growth—additive manufacturing, robotics and surface...
ApiFix System Reaches 250-Patient Milestone in Scoliosis Correction
The ApiFix Minimally Invasive Deformity Correction (MID-C) technology for correction of Adolescent Idiopathic Scoliosis
Amedica Closes Sale of Spine Portfolio to CTL Medical
Amedica completed the sale of its spine business to CTL Medical, which is now exclusive owner of the metal and sil...
SI-BONE Announces UK Guidance Recommendation for iFuse
The U.K.'s National Institute for Health and Care Excellence published medical technology guidance recommending SI-BONE's iFuse
Medacta Appoints New CEO, Francesco Siccardi
Medacta's current Executive Vice President, Francesco Siccardi, will become the company's next chief executive officer
Vertos Medical Enrolls in New MOTION Study of MILD Procedure
Vertos Medical enrolled the first patient into MOTION, a new multicenter two-year U.S. study of the mild
Kuros Biosciences: First Procedure in MagnetOS Spinal Fusion Trial
The first patient has been treated in a multicenter study comparing Kuros Bioscience's MagnetOs bone graft substitute vs. autolo...
FDA Approves Update of Mobi-C Cervical Disc Labeling to Include 7-Year Clinical Results
FDA approved an update to the labeling for Zimmer Biomet’s Mobi-C® Cervical Disc to include 7-year clinical results, showing the devi...
Alphatec Gains FDA Clearance for OsseoScrew
Alphatec received FDA 510(k) clearance to market the OsseoScrew® expandable pedicle screw. 
Baxter Receives FDA Clearance for ALTAPORE Bone Graft
Baxter was granted FDA 510(k) clearance to market ALTAPORE Bioactive Bone Graft as an autograft extender...
Renovis Surgical Receives FDA Clearance for Tesera X Lateral Interbody Fusion System
Renovis Surgical received FDA 510(k) clearance to market the Tesera® X Lateral Interbody Fusi...
LifeNet Health Launches PliaFX Prime Cortical Fibers
LifeNet Health commenced limited launch of PliaFX® Prime precision-engineered cortical fibers.
NuVasive Enrolls Patients in Advanced Materials Science in XLIF Study
NuVasive commenced patient enrollment in a prospective, multicenter U.S. study evaluating advanced spinal impla...
DePuy Synthes Launches SENTIO Nerve Monitoring Technology
DePuy Synthes introduced SENTIO MMG, a digital system to assess nerve status and identify and avoid peripheral nerves ...
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