ORTHOFLASH®

The world's first TKA was performed using the STELLAR Knee mixed-reality surgical guidance system from PolarisAR.

First Total Knee with STELLAR Mixed-reality Surgical Guidance

The world’s first TKA was performed using the STELLAR Knee mixed-reality surgical guidance system from PolarisAR.

Trivicta's triple-taper femoral stem supports an optimal fit within the canal for a diverse range of patient anatomies.

Ortho Development Gains FDA Clearance on Trivicta Hip

Trivicta’s triple-taper femoral stem supports an optimal fit within the canal for a diverse range of patient anatomies.

BioPoly Radial Head

BioPoly Radial Head Receives FDA Clearance

This implant is manufactured from BioPoly’s proprietary material and is reported to be the only synthetic cartilage Radial Head on the market.

First Total Knee with STELLAR Mixed-reality Surgical Guidance

The world’s first TKA was performed using the STELLAR Knee mixed-reality surgical guidance system from PolarisAR.

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Ortho Development Gains FDA Clearance on Trivicta Hip

Trivicta’s triple-taper femoral stem supports an optimal fit within the canal for a diverse range of patient anatomies.

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BioPoly Radial Head Receives FDA Clearance

This implant is manufactured from BioPoly’s proprietary material and is reported to be the only synthetic cartilage Radial Head on the market.

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Bioretec RemeOs Granted Breakthrough Device Designation

RemeOs Spinal Interbody Cages are intended to restore intervertebral height and facilitate intervertebral body fusion in the cervical spine.

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CERAMENT G Gains FDA 510(k) for Open Fracture Treatment

BONESUPPORT’s CERAMENT G synthetic bone graft substitute received FDA marketing clearance for use in open fractures.

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Ventris Gains Additional Clearance for Amplify Synthetic Bone Graft Putty

FDA granted 510(k) marketing clearance in the intervertebral disc space for Amplify Synthetic Bone Graft Putty.

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Regulatory Approval for Intellijoint KNEE in Japan

Intellijoint KNEE is enabling technology, providing real-time measurements of surgical cutting guides during total knee replacement.

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Medtronic Launches UNiD ePRO Service in the United States

Medtronic partnered with OBERD, a practice intelligence data collection company, to provide spine surgeons with an electronic Patient Reported Outcomes system.

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Spineart Completes Enrollment for Baguera-C 2-Level Disc Trial

The U.S. IDE trial will study the Baguera-C Disc in patients with cervical disc disease at two contiguous levels.

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SurGenTec Gains FDA Clearance for OsteoFlo HydroPutty

HydroPutty bone graft features hydrophilic carriers designed to absorb fluids such as bone marrow aspirate, blood or saline.

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Sonex Enrolls to Study Carpal Tunnel Release

Sonex launched a clinical registry to collect real-world data on patients treated with carpal tunnel release using ultrasound guidance.

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BONESUPPORT Gains 510(k) for Cerament in Interbody Fusion

CERAMENT bone void filler is an injectable, moldable and drillable synthetic bone void filler comprising hydroxyapatite and calcium sulfate.

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OrthoPediatrics Launches RESPONSE Rib and Pelvic Fixation for EOS Scoliosis

This is the company’s first solution to treat Early Onset Scoliosis patients, specifically those associated with or at risk of Thoracic Insufficiency Syndrome.

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Spineart Completes Enrollment in Baguera C IDE Trial for Single-level Cervical Disc Replacement

Baguera C has been commercially available in select European and worldwide markets since 2008, with over 60,000 implants sold.

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Risk Reduction in Spinal Fusion with Kleiner Device Labs’ KG2 Surge

KG2 Surge is a single-patient-use bone graft delivery tool coupled with a 3D-printed titanium I-Beam fusion implant.

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