Cervical Spine

The company announced it acquired Simplify Medical for $150 million in cash along with future regulatory and sales milestones.

The 50-patient study will support an application for clearance of anterior cervical plates and interbody cages for commercial use.

The system features a titanium plate PEEK cage with cortical cancellous screws and a large cavity for autogenous bone graft.

This is NGMedical's first FDA clearance for its spinal devices.

The multicenter study will examine efficacy of the Synergy Disc vs. anterior cervical discectomy and fusion in patients with degenerative disc disease.

icotec's Anterior Cervical Plate is the only 100% nonmetallic and radiolucent ACP with a plate and screws made of Carbon/PEEK available in the U.S.

The latest 510(k) for the Tiger Shark Cervical Spacer addresses sizes that enhance the ability to treat a wider variety of patient anatomies.

SPIRA Lateral 3.0 implant is a titanium open architecture LLIF utilizing Camber's Surface by Design technology to optimize bone growth.

This is the first implantation of Simplify's Cervical Artificial Disc following 1-level approval from FDA.

BEE HA is an anatomically shaped cervical interbody made of PEEK-OPTIMA™ Hydroxyapatite Enhanced material developed by Invibio.

The newest product in the MIS Ultra suite of products is aimed at minimizing the unintended consequences of traditional spine surgery.

Admiral ACP represents next-gen anterior cervical plating, designed to yield an optimal balance among strength, profile and construct rigidity.

The debut includes commercial launch of the Anterior Cervical Plating system, featuring the thinnest plate on the market at 1.6 mm.

Following acquisition of parent company FH Ortho, Spine Innovations is fully independent and dedicated to worldwide sales deployment of ESP disc replacements.

Astura Medical was granted FDA 510(k) clearance to market the Dolomite Stand-Alone Anterior Cervical Stabilization System. Dolomite is the company's third technology providing a combined interbody and fixation option to receive 510k approval within the last 6 months....

Simplify Disc is designed for MRI compatibility, physiologic motion and anatomical height-matching to improve patient outcomes and expand treatment options.

ReVivo Medical is developing elastic micro-motion implantable spinal devices.

The AIS-C 3DP Stand-Alone Cervical Cage is combined with titanium anchors enabling bony fusion and fixation with direct anterior access.

The Orthofix O-GENESIS Graft Delivery System features a new hydrated, ready-to-use AlloQuent Structural Allograft Q-PACK.

The company posted 2018 and 2019 revenue of $90.8 million and $95.9 million, respectively, growing +5.6% year over year.

The companies will develop single-use instrumentation for cervical spine procedures suitable for acute care hospitals, outpatient hospitals and ASCs.

Study results demonstrated that the Simplify Disc achieved superiority in overall success compared to anterior cervical discectomy and fusion.

The Turn Lock System features the dual functionality of a cervical interbody and anterior plate with an integrated one step turn lock.

Using NanoMetalene Technology, Reef Topography and a TruProfile plating system, Shoreline RT provides complete intraoperative choices for spinal fusion.

The JASPIS ST spinal disc replacement has been developed specifically for the requirements of anterior cervical vertebral fusion.

The HiJAK SA Expandable Cervical Stand-Alone Interbody system is the company's second first-to-market expandable system in just 18 months.

Co-developed with Sagitechnology, A-CIFT is the first ever HA impregnated standalone cervical cage for greater sagittal correction.

The single-level trial will compare the BAGUERA C Cervical Disc Prothesis to another FDA approved arthroplasty device at up to 30 U.S. sites.

The patent claims provide broad protections for material and manufacturing that support fully porous, bioactive polyetheretherketone technology.

While MIS procedures typically focus on incision size, MIS Ultra considers post-op implications such as disruption of skeletal and muscle tissue.

F3D-C2 features the only 3D-printed technology with both a trabecular structure and directional support lattices.

ShurFit 2C features a coating of titanium and hydroxyapatite to help increase durability support fixation during biologic fusion.

FDA has determined that the premarket approval is complete, and has commenced the filing review for the 1-level cervical disc.

HiJAK SA joins first-to-market HiJAK AC and the V3 segmental plating system as the latest technology in Atlas Spine's disruptive design portfolio.