SpineNET Single Screw Plate

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.

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

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.

Stryker Q Guidance System

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.

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.

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.

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.

Acumed Hits Milestone with Acu-Loc Wrist Plating

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

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.

Zimmer Biomet Receives FDA Clearance for Identity Shoulder

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

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.

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.

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.

First Cases with Anika’s X-Twist Fixation System

The suture anchor system is suitable for repairs in the shoulder, foot/ankle and other extremities.

First Clinical Use of Medartis StealthFix Fixation

StealthFix is a zero-profile intraosseous fixation solution with multiple applications in the forefoot and midfoot.

Stryker Launches Pulse Intelligent Delivery Platform

Pulse Intelligent Delivery provides an integrated product configuration and delivery offering for foot/ankle surgery within the ASC setting.

CTL Amedica Granted Taiwan License for MATISSE ACIF Cage

The MATISSE ACIF Cage features streamlined instrumentation and a tapered leading edge for easy insertion, as well as a large graft area.

Smith+Nephew REGENETEN Bioinductive Implant Study Update

Interim analysis from a randomized controlled trial shows a significant reduction in the re-tear rate of full-thickness rotator cuff repairs.

Ventris Medical Granted 510(k) for Amplify Synthetic Bone Graft Putty

Amplify represents a new class of synthetic biomaterials designed for the optimization of cell proliferation and bone formation.


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