EOS imaging will present its EOSapps solution at the French Society of Orthopedic and Traumatological Surgery Congress, Nov. 12-15, at the Palais des Congrès in Paris, France.

K2M received FDA 510(k) clearance for surgical guidance that enhances its Mesa Platform Technology using patient-specific rods and rails.

Alkaline-treated silk fibroin/calcium phosphate cement may be a reliable composite bone cement for minimally invasive orthopedic surgeries, according to a study in International Journal of Nanomedicine.

NuVasive received FDA 510(k) clearance for the use of its Cohere Porous PEEK implant in eXtreme lateral interbody fusion procedures.

Spinal Elements received FDA clearance for claims related to its Ti-Bond titanium surface coating technology.

Titan Spine closed a series B financing round, with current investment partner Southlake Equity Group leading the round.

Apium Additive Technologies' medical PEEK 3D printing application on the Apium M220 Series machine has met biocompatibility criteria for skull and hand implants, 3D Printing Industry reports.

Zimmer Biomet received FDA 510(k) clearance for its Persona Revision Knee System.

Innovasive received FDA 510(k) clearance for its DualX technology.

Richard Weiner, MD, and Bryan Barnes, MD, performed the first cases using Life Spine's Prolift Post Pack Expandable Interbody System.

Porous PEEK improves the bone-implant interface compared to plasma-sprayed, titanium-coated PEEK, according to a study in Biomaterials.

Three professors in UC San Francisco School of Medicine's orthopedic surgery department founded EDGE Labs to make 3D printing more accessible.

Camber Spine has generated $1 million from the Spira-C interbody device within six months of its commercial launch.

DJO's Empowr 3D Knee technology improves function and patient satisfaction after total knee arthroplasty surgery, according to a study in Techniques in Orthopaedics. 

Medacta International launched a patient-matched posterior lumbar fusion solution at the North American Spine Society 2018 Annual Meeting in Los Angeles, Sept. 26-29.

Synoste raised $5.8 million to launch its smart skeletal deformation correction technology for orthopedic and spine applications.

SpineEx earned FDA 510(k) clearance for its Sagittae lateral lumbar interbody fusion device.

Ortho Development Corp. signed an exclusive agreement with DePuy Synthes, part of Johnson & Johnson Medical Device Companies, to promote its KASM Knee Articulating Spacer Mold in the U.S.

CoreLink Surgical received FDA 510(k) clearance for its M3 Stand-Alone Anterior Lumbar Interbody Fusion System.

Medacta International received FDA 510(k) clearance for its Mpact 3D Metal Implants and Augments 3D Metal as enhancements to its Mpact System for primary to complex hip revision procedures.