Julie Vetalice, Author at ORTHOWORLD

OrthoPediatrics Announces Expanded Indication for FIREFLY Pedicle Screw Navigation

OrthoPediatrics announced an additional FDA 510(k) clearance for the FIREFLY® Pedicle Screw Navigation Guide to include S2AI screw trajectory for sacral-iliac fixation in complex spinal reconstruction.

Aug 01, 2018

SeaSpine 2Q18 Revenue +7% vs. 2Q17

Company Revenue The Numbers

SeaSpine announced 2Q18 revenue of US $36.4MM, +6.5% vs. 2Q17, and 1H18 revenue of $69.6MM, +5.3% vs. 1H17. This is the company's highest quarterly growth rate since its spinoff from Integra LifeSciences in 2015.

Aug 01, 2018

Zimmer Biomet Ortho Revenue +4% vs. 2Q17

Company Revenue The Numbers

ORTHOWORLD estimates Zimmer Biomet 2Q18 orthopaedic revenue of US $1,858.2MM, +3.5% vs. 2Q17, and 1H18 revenue of $3,714.8MM, +2.8% vs. 1H17.

Aug 01, 2018

Episurf Hears FDA Feedback on IDE for Episealer Knee

Joint Replacement ORTHOFLASH

Episurf Medical is entering its next phase on its IDE application to initiate a U.S. clinical study of the Episealer® knee implant.

Jul 30, 2018

Anika Therapeutics 2Q18 Orthobiologics Revenue +7% YoY

Company Revenue The Numbers

Anika Therapeutics posted 2Q18 orthobiologic revenue of US $26.2MM, +7.0% vs. 2Q17 and 1H18 revenue of $45.7MM, +2.2% vs. 1H17.

Jul 30, 2018

Cerapedics Enrolls Patients in IDE Study of P-15L Bone Graft in TLIF

Orthobiologics ORTHOFLASH

Cerapedics enrolled the first patients in an IDE clinical trial evaluating P-15L Bone Graft vs. autograft in TLIF.

Jul 30, 2018

Integra LifeSciences Reports 2Q18 Revenue

Company Revenue The Numbers

ORTHOWORLD estimates Integra LifeSciences' 2Q18 orthopaedic revenue at US $30.4MM, -0.6% vs. 2Q17, and 1H18 revenue of $55.2MM, -2.5% vs. 1H17.

Jul 30, 2018

Smith & Nephew Posts 2Q18 Ortho Revenue Growth +4% YoY

Company Revenue The Numbers

ORTHOWORLD estimates Smith & Nephew 2Q18 orthopaedic revenue of US $870.8MM, +4.4% from 2Q17, and 1H18 revenue of $1,736.1MM, +4.5% vs. 1H17.

Jul 30, 2018

CarboFix Gains FDA Clearance for Pedicle Screw

ORTHOFLASH Spine

CarboFix Orthopedics received FDA 510(k) clearance to market the CarboClear® Carbon Fiber Pedicle Screw to treat oncological patients.

Jul 27, 2018

NuVasive Gains FDA Clearance for Pulse Surgical Automation

ORTHOFLASH Robotics/Tech

NuVasive received FDA 510(k) clearance to market Pulse surgical automation, the foundation for the company's Surgical Intelligence system.

Jul 27, 2018

Get the ORTHOWORLD Newsletter!

Contact Us