Spine

Precision Spine Announces FDA Clearance of its ShurFit ACIF 2C System

Precision Spine, Inc. has recently announced that it has received 510(k) clearance of its ShurFit ACIF 2C Anterior Cervical Interbody System, which is made from medical grade polyetheretherketone (Peek Optima, LT1) and coated with both commercially pure Titanium (Ti) and Hydroxyapatite (HA).

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SeaSpine Announces 510(k) FDA Clearance for its Mariner Posterior Fixation System

The Mariner Posterior Fixation System is a pedicle screw system featuring modular threaded technology and accompanying instrumentation. Designed to reduce the number of trays needed for surgery, Mariner is intended to provide surgeons with multiple intra-operative options to facilitate posterior lumbar fixation.

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Meditech Spine Receives FDA Clearance for the CURE Anterior Cervical Plate System

Meditech Spine has received the US Federal Drug Administration (FDA) 510(k) clearance to market the the CURE Anterior Cervical Plate to complement its Talos®-C (HA) line of interbody devices.

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iData Spine Interbody Fusion Devices News Roundup: New Spinal Elements, SeaSpine Products

Recently, there has been lots of exciting developments in the minimally invasive surgery (MIS) interbody fusion device market. Here is a pair of announcements in the industry we would like to highlight.

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Medtronic, NuVasive Lead MIS Interbody Fusion Market Driven by Positive Procedure Outcomes

The MIS interbody fusion market in the U.S. is expected to exceed $1.15 billion by 2021; this market has continued to experience high growth rates in comparison with the traditional spine markets.

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Interventional Spine, Inc. Announces New Line of Opticage Lumbar Interbody Fusion Implants

Interventional Spine, Inc. announced the launch of a new line of products which include recent size additions to the Opticage® Lumbar Fusion line of spine products, as well as lordotic versions of the interbody device

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New Low-cost Spinal Fusion Device to Reduce Chronic Back Pain

Researchers anticipate the innovative medical device, called Thru-Fuze, will transform spinal fusion surgery, which is used when conservative therapies such as physical therapy, medication and injections have failed.

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FDA Approves First Load-Bearing 3D-Printed Spinal Implant Device

The Food and Drug Association recently cleared the SpineFab vertebral body replacement (VBR) system by Oxford Performance Materials (OPM). This is the first 3D-printed spinal implant device to be cleared for a load-bearing indication and is suitable for long-term use in patients.

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Zimmer, Biomet and Lima Mergers and Acquisitions in the European Orthopedic Market

According to a recent report by iData Research, Zimmer is one of the leading competitors in the European minimally invasive spinal implant market. The company competed in both segments and markets its products in this area under its own spine division.

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Boston Scientific Releases the World’s Smallest Spinal Cord Stimulator in Europe

The Precision Novi spinal cord stimulation system by Boston Scientific, a device to manage chronic pain, is now available in Europe. Spinal stimulators alleviate pain by using stimulation therapy to reduce nerve fiber pain signals.

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