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2017

Spineology® Announces FDA Clearance of Rampart One™ Anterior Lumbar Interbody Fusion System

ST. PAUL, Minn.--( BUSINESS WIRE )--Spineology, Inc. the innovator in anatomy-conserving surgery™, is excited to announce FDA clearance of the Rampart One Anterior Lumbar Interbody Fusion System. Rampart One is designed to minimize the exposure and vascular retraction requirements associated with traditional anterior spinal fusion procedures. The system includes both standard and oblique interbody device footprints each with integrated fixation screws. “Minimizing exposure and retraction are cornerstone elements of all Spineology anatomy conserving designs. We are very excited about this approval and look forward to entering the anterior market in the near future,” said John Booth CEO of Spineology. “Variable...

Spineology® Announces Expanded FDA Clearance of Elite™Expandable Interbody Fusion System

Spineology, Inc. the innovator in Anatomy-Conserving Surgery™, is excited to announce expanded FDA clearance of the Elite Expandable Interbody Fusion System. Included in the clearance is the addition of a narrower, 10mm, version of the device and an indication to utilize the devices with allograft bone. “The broader size offering and the allograft bone indication allow the surgeon to pair Elite with Incite™ Cortical Fibers, said John Booth, CEO of Spineology. “Incite’s excellent handling properties and ability to expand in-situ with the Elite Implant are added benefits not found in competitive systems.” “The Elite Expandable Interbody device is an ideal...

ConneX Cross Connectors and Rod Connectors

ST. PAUL, Minn. Spineology Inc., an innovator in anatomy-conserving spine surgery, announced today the launch of the ConneX™ Cross Connector and ConneX™ Rod Connectors to support their expanding line of pedicular fixation systems. ConneX Connectors offer surgeons a versatile, user friendly cross connector option that accommodates 4.75mm and 5.5mm diameter rods, comes in a variety of lengths, and has a unique rod clamp design to eliminate high stress point loading while maximizing fixation to the rod. “The ConneX Connector set includes a variety of connector options to meet the high demands of revision surgery and includes options to accommodate both...

Spineology® Receives $5 million Investment from Hermed Capital

ST. PAUL, Minn. Spineology Inc., the innovator in anatomy-conserving surgery™, is pleased to announce that Hermed Capital, a private equity fund located in Shanghai, China, has made a $5 million investment in the form of a convertible debenture. The proceeds from this financing are expected to fund additional commercialization, product development, and clinical research efforts for the company. "We believe the Spineology investment is a very exciting opportunity," stated Dr. Jerry Xiao, Managing Director of Hermed Capital. "Spineology possess a very novel product portfolio in an otherwise very homogeneous market. We look forward to working with them as they grow...

Spineology® Initiates Full Market Release of Elite™ Expandable Interbody Fusion System

Spineology, Inc. an innovator in Anatomy-Conserving Surgery™, is pleased to announce the full market release of the Elite Expandable Interbody Fusion System. Over 300 cases have been completed using Elite and system utilization continues to accelerate as the full market release of Elite is initiated. “Following the successful completion of the Elite Expandable Interbody Fusion system limited release and the receipt earlier this year of the expanded FDA clearance, which included the addition of a narrower 10mm footprint and allograft bone labeling, we have now initiated the full market release of Elite”, said John Booth, CEO of Spineology. “The Implant’s...

Spineology Initiates Post-Market Lateral Interbody Fusion Study Using Novel Implant Design

ST. PAUL, Minn. – Spineology Inc., the innovator in anatomy-conserving spine surgery, has announced the initiation of a prospective, post-market lateral interbody fusion study designed to evaluate patient outcomes using its FDA-cleared Duo™ Lumbar Interbody Fusion System. The Duo System offers a unique implant design that is the first to combine PEEK, titanium, and graft containment mesh elements. The design dramatically reduces the access required to implant a device compared to traditional lateral systems. By minimizing the nerve and soft tissue retraction typically required in these surgeries, the company believes the Duo System can reduce the post-operative thigh pain and...

Spineology to Highlight Novel Lateral Interbody Fusion System at NASS

ST. PAUL, Minn. – Spineology Inc., the innovator in anatomy-conserving spine surgery, announced today the company will be highlighting their unique, recently FDA-cleared Duo™ Lumbar Interbody Fusion System at the North American Spine Society (NASS) annual meeting in Orlando, Florida. The Duo System features the first lateral implant to combine PEEK, titanium, and the company’s proprietary mesh technology. The unique design dramatically reduces the access required to implant a device compared to traditional lateral systems. By minimizing the nerve and soft tissue retraction typically required in these surgeries, the company believes the Duo System can reduce the post-operative thigh pain...