Interbody Devices Market Analysis | United States | 2019-2025 | MedCore
- Year: 2017
- Scope: 2013-2023
- Region: United States
- Pages: 571
- Published Date: 4/1/2017
- Type: MedCore
The advent of more high quality and innovative motion preservation and MIS technologies is expected to contribute to this decelerating growth over the forecast period. The most notable of these technologies are cervical artificial discs and MIS sacroiliac joint fusion implant systems, the markets for both of which are expected to grow rapidly. Nevertheless, the total interbody device market is expected to increase.
Interbody (IB) devices are designed to replace the intervertebral discs of the spine, which enhances stability in the region and promotes fusion between the two vertebral bodies. These devices are threaded, allowing them to be used in conjunction with bone graft material. Over time, the packed graft is gradually replaced by natural bone, forming a solid piece. IB fusion procedures typically add a posterior fixation device to the associated level.
Segments Covered in This Market
- Total Interbody Device Market (ALIF, PLIF, TLIF, CIF, VBR/Corpectomy, Expandable, Standalone)
Report Data Types Included
- Unit Sales, Average Selling Prices, Market Value & Growth Trends
- 10 Year Scope (3 Year Historical + 7 Year Forecast Period)
- Market Drivers & Limiters for Each Segment
- Competitive Analysis with Market Shares
- Product Portfolios
- Related Press Releases from Top Competitors
Companies Analyzed
In 2016, the leading competitor in the U.S. interbody device market was DePuy Synthes. The company offers its radiolucent lumbar interbody fusion cages made of carbon fiber reinforced polymer (CFRP) in addition to several other mesh and non-bone devices. Medtronic led the non-bone interbody device segment with their LT-Cage® and INTER FIX cages. Stryker was the third leading competitor in bone and non-bone interbody devices, as well as in VBR/corpectomy devices and expandable devices; these positions were derived from their comprehensive line of PEEK and titanium metal implants. Other companies analyzed include Globus Medical, Zimmer Biomet, NuVasive, Alphatec Spine, K2M, Seaspine, Centinel Spine, Titan Spine and Amedica.
About Our In-Depth MedCore Research
Our analysts meticulously research for up to 3 to 4 months to put together one suite of reports (MedSuite), which is a comprehensive analysis on a group of healthcare markets. A MedCore is one portion of that analysis that focuses on one market segment, and provides further detailed segmentation to get a much more granular set of market data.
This MedCore is also found in the full report suite titled U.S. Market Report Suite for Spinal Implants and VCF – MedSuite
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- Strong foundation of quantitative and qualitative research
- Focused on the needs and strategic challenges of the industry participants
Step 1: Project Initiation & Team Selection During this preliminary investigation, all staff members involved in the industry discusses the topic in detail.
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Step 5: Research Analysis: Establishing Baseline Estimates Following the completion of the primary research phase, the collected information must be synthesized into an accurate view of the market status. The most important question is the current state of the market.
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Interbody Devices Market Analysis | United States | 2019-2025 | MedCore
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Interbody (IB) devices are designed to replace the intervertebral discs of the spine, which enhances stability in the region and promotes fusion between the two vertebral bodies. These devices are threaded, allowing them to be used in conjunction with bone graft material. Over time, the packed graft is gradually replaced by natural bone, forming a solid piece. IB fusion procedures typically add a posterior fixation device to the associated level. These procedures are often referred to as 360° fusions, as surgeons will implant interbody devices from an anterior approach and flip the patient over to implant a posterior pedicle screw device. This combination increases the fusion success rate over an interbody fusion device implantation without the addition of fixation devices.
- 2017
- 2013-2023
- United States
- 4/1/2017
- 571
- MedCore
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