ORTHOFLASH®

Aurora Spine SiLO TFX

Aurora Spine Gains FDA 510(k) Clearance for SiLO TFX

The SiLO TFX MIS Sacroiliac Joint Fixation System is intended to treat conditions including sacroiliac joint disruptions and degenerative sacroiliitis.

HAPPE material offers interconnected, cancellous porosity and bioactive surfaces with exposed hydroxyapatite to enable robust bone in-growth and on-growth.

HAPPE Spine Gains Additional Patents for Hydroxyapatite Devices

HAPPE material offers interconnected, cancellous porosity and bioactive surfaces with exposed hydroxyapatite to enable robust bone in-growth and on-growth.

GHOST 3D-Printed Titanium Spacers expand on Life Spine’s interbody portfolio, comprising PEEK, titanium and now 3D-printed titanium spacers.

Life Spine Gains FDA 510(k) Clearance for GHOST Spinal Spacer

GHOST 3D-Printed Titanium Spacers expand on Life Spine’s interbody portfolio, comprising PEEK, titanium and now 3D-printed titanium spacers.

First MySpine Anchor Procedure Completed in the US

MySpine Anchor, the latest addition to the MySpine platform, is Medacta’s patient-matched solution for posterior sacro-iliac joint fixation.

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Stryker Launches Monterey AL Interbody with New Pre-clinical Data

Monterey AL Interbody System, a stand-alone interbody fusion device, is designed for anterior lumbar interbody fusion.

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Trice Medical Partners to Expand Diagnostic Platform

The mi-ultra with mi-tablet 3 is a diagnostic and therapeutic visualization technology that provides two clear ways to see into the body on the same tablet.

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SpineNet Launches SSP – Single Screw Plate

The SSP Anterior Cervical Plate system requires only a single screw per vertebrae level, and is available for multiple levels in an extensive range of sizes.

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NuVasive Launches Reline Cervical for Posterior Cervical Fusion

This marks the completion of the NuVasive Reline fixation portfolio for complex deformity, from occiput to sacrum.

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Stryker Launches Q Guidance System for Spine

Q Guidance combines new optical tracking options with a redesigned camera and sophisticated algorithms to deliver more planning and navigation capability than before.

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First Knee Revisions with Smith+Nephew CORI

Smith+Nephew is reportedly the the first to receive FDA 510(k) clearance for a revision indication using a robotics-assisted platform.

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Surgalign Launches Fortilink with TiPlus Technology Portfolio

The Fortilink interbody product line now include both titanium and 3D-printed polymer options for anterior and posterior lumbar interbody fusion and ACDF.

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Moximed’s MISHA Knee Achieves Superiority of Primary Endpoint in Pivotal Study

MISHA is reported to be the world’s first implantable shock absorber for the knee.

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Acumed Hits Milestone with Acu-Loc Wrist Plating

The one millionth Acu-Loc device was implanted in the treatment of a distal radius fracture.

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First U.S. Revision Cases with Medacta MyKnee R

MyKnee R provides personalized 3D interactive preoperative planning and a set of 3D-printed guide blocks for use in revision knee procedures.

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Zimmer Biomet Receives FDA Clearance for Identity Shoulder

Identity is a convertible, adaptable system for anatomic, reverse and revision shoulder replacement.

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Smith+Nephew Launches OR3O Dual Mobility System in Japan

OR3O Dual Mobility is available in Japan for primary and revision applications and is compatible with the R3 Acetabular System.

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First U.S. Surgical Case with Lazurite ArthroFree System

ArthroFree is the first fully wireless camera for arthroscopy and general endoscopy to receive market clearance from FDA.

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Stryker Gains FDA 510(k) for OptaBlate Bone Tumor Ablation

OptaBlate completes Stryker’s Interventional Spine portfolio of treatment options for metastatic vertebral body fractures.

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