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Spine Procedures, Practices and News
A Los Angeles County Superior Court jury has ordered Johnson & Johnson's DePuy orthopedic device unit to pay more than $8 million to the plaintiff in the first of approximately 11,000 lawsuits over the company's metal-on-metal hip implants, according to JD Journal.
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Spine and Orthopedic Devices and Implants
March 08, 2013
6 Orthopedic & Spine Device Company Mergers or Acquisitions
Here are 6 recent orthopedic and spine device company mergers or acquisitions.
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Spine and Orthopedic Devices and Implants
March 06, 2013
TranS1 Posts $12M 4Q Loss
TranS1 medical device company posted a net loss of $12 million for the fourth quarter of 2012, due in part to increased operating expenses from a government settlement.
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Spine and Orthopedic Devices and Implants
March 05, 2013
AxoGen Names Shawn McCarrey as Senior VP of Sales
Alachua, Fla.-based AxoGen appointed Shawn McCarrey as its senior vice president of sales.
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Spine and Orthopedic Devices and Implants
March 01, 2013
12 News Updates for Orthopedic & Spine Device Companies
Here are 12 recent news updates for orthopedic and spine device companies in the month of February.
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Spine and Orthopedic Devices and Implants
March 01, 2013
ArthroCare SpeedLock Hip Implant Cleared by FDA
The FDA granted clearance to ArthroCare's SpeedLock HIP Knotless Fixation implant.
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Spine and Orthopedic Devices and Implants
February 28, 2013
Vexim Acquires Orthopedic Cement Injection Technology
The Balma, France-based medical device company Vexim has acquired a system to mix and inject orthopedic cement for vertebroplasty procedures.
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Spine and Orthopedic Devices and Implants
February 28, 2013
MAKO Surgical Loses $5.7M in 4Q 2012 From Fewer Robotic Device Sales
MAKO Surgical suffered a net loss of $5.7 million in the fourth quarter of 2012, and the company's revenue for the quarter declined 8 percent from $32.9 million in 2011 to $30.2 million in 2012 due to down device sales.
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Spine and Orthopedic Devices and Implants
February 25, 2013
FDA Issues Class 1 Recall for DePuy Revision Knee Device
The FDA issued a Class 1 recall for DePuy Orthopaedics’ LPS Diaphyseal Sleeve, which is used with the LPS system as an end-stage revision knee device.
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Spine and Orthopedic Devices and Implants
February 21, 2013
Smith & Nephew Names Dr. Michael Friedman to Board of Directors
Global medical device company Smith & Nephew named Michael Friedman, MD, as a non-executive director to join the board April 11.
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Spine and Orthopedic Devices and Implants




