Cutting Edge Spine
Manufacturing · North Carolina, United States · 1-10 Employees
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Overview
Headquarters
6012 Waxhaw Hwy, Mineral Springs, North ...Phone Number
(704) 243-0892Website
www.cuttingedgespine.comRevenue
<$5 MillionIndustry
About Cutting Edge Spine
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Debt
$150K
Cutting Edge Spine Tech Stack
A closer look at the technologies used by Cutting Edge Spine
Cutting Edge Spine News & Media
Cutting Edge Spine Announces FDA 510(k) Clearance of T-FIX 3DSI Joint Fusion System with Proprietary Trabecular Technology
The T-FIX 3DSI Joint Fusion System is the first of many systems from Cutting Edge Spine to implement proprietary trabecular fixation platform. (PRWeb July 14, 2022) Read the full story at https://www.prweb.com/releases/2022/07/prweb18786834.htmCutting Edge Spine Announces Notice of Issuance from the U.S. Patent...
This patent issuance solidifies Cutting Edge Spine as an industry leader in 3D printed trabecular fixation for orthopedic applications. (PRWeb June 24, 2021) Read the full story at https://www.prweb.com/releases/cutting_edge_spine_announces_notice_of_issuance_from_the_u_s_patent_and_trademark_office_regarding_patent_no_us_10_993_754_b2_implants_for_tissue_fixation_and_fusion/prweb18014416.htmCutting Edge Spine Announces FDA 510(K) Clearance of its New HA Enhanced PEEK Interbody System for a Direct Lateral Approach to the Spine, the EVOL®ha-DLIF
The commercial launch of the EVOL®ha-DLIF, a PEEK-OPTIMA HA Enhanced direct lateral interbody fusion system, signals the latest in a broad portfolio of bioactive interbody systems from Cutting Edge Spine. (PRWeb January 09, 2020) Read the full story at https://www.prweb.com/releases/cutting_edge_spine_announces_fda_510k_clearance_of_its_new_ha_enhanced_peek_interbody_system_for_a_direct_lateral_approach_to_the_spine_the_evolha_dlif/prweb16821645.htmCutting Edge Spine Announces FDA 510(K) Clearance of its EVOL-SI Joint Fusion System; Bringing Novel Super Hydrophilic Nano-technology to the Sacral-iliac Fixation Market
The commercialization of the EVOL-SI system addresses the needs of orthopedic surgeons and neurosurgeons seeking superior clinical outcomes following sacral-iliac surgery. (PRWeb August 20, 2019) Read the full story at https://www.prweb.com/releases/cutting_edge_spine_announces_fda_510k_clearance_of_its_evol_si_joint_fusion_system_bringing_novel_super_hydrophilic_nano_technology_to_the_sacral_iliac_fixation_market/prweb16509505.htm
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Frequently Asked Questions Regarding Cutting Edge Spine
Cutting Edge Spine is a privately owned medical device organization founded in 2009, headquartered in North Carolina. The company specializes in developing and commercializing innovative orthopedic fixation systems, particularly in spinal technologies, with a focus on improving clinical outcomes. They hold an extensive patent portfolio for trabecul... Read More