Global XLIF Surgery Market is expected to reach USD 2,557.74 million by 2024 from USD 1,644.68 million in 2016, at a CAGR of 5.7% in the forecast period 2017 to 2024. The new market report contains data for historic years 2015, the base year of calculation is 2016 and the forecast period is 2017 to 2024.
The Global XLIF Surgery Market is highly concentrated to a few big players and rest to local players who cater to domestic markets only. NuVasive Inc. is going to dominate the global XLIF surgery market following with, RTI Surgical Inc. and K2M,Inc.

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Players in global XLIF surgery market
• Spine Wave, Inc.,
• Tyber Medical LLC.,
• K2M, Inc.,
• Johnson & Johnson Services Inc.,
• Titan Spine,
• DIO MEDICAL,
• OsteoMed,
• ZIMMER BIOMET

Among others holds 26.6% of the global XLIF surgery market in 2016.

NUVASIVE INC.:
Incorporated in 1997 and headquartered at San Diego, California, United States. The company is medical device company in the global spine surgery market. It develops minimally-disruptive surgical products and procedurally-integrated solutions for spine surgery. Its wide range of products is focused on various applications of spine fusion surgery and spinal fusion process.
NuVasive Inc. operates its business through one segment. It reports in two product lines namely, spinal hardware and surgical support.

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RTI Surgical Inc. :
Founded in 1997 and headquartered at Alachua, Florida, U.S., RTI Surgicals, Inc., is engaged in the development and marketing of biologic, metal, and synthetic implants. The company operates through four business segments, namely, spine, sports medicine and orthopedics, surgical specialties and cardiothoracic.
The spine product category of the company offers various products pertaining to cervical, lateral, orthobiologics and thoracolumbar. It offers the products Fusion Lateral Disc Prep Set, Lat-Fuse Lateral Plate System, MIS Fusion Instrument Set, Clarity Retractor System and many others.

Recent Development: Global XLIF Surgery Market
1. In July 2017, K2M Group Holdings, Inc. signed the agreement with Mitsubishi Corporation subsidiary Japan Medicalnext Co., Ltd. for the distribution of K2M’s innovative spinal technologies in Japan.
2. In October 2016, K2M Group Holdings, Inc. received 510(k) clearance from FDA for the expansion of the CASCADIA Lateral Interbody System, which consists of the Lamellar 3D Titanium Technology. The CASCADIA Lateral Interbody System expanded the portfolio of the company for the minimally invasive surgery products
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