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Extreme Fixes for Orthopedic Extremity Surgery
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Siemens Healthineers Gains FDA Clearance for MAGNETOM Terra.X
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ODT's Most-Read Stories This Week—March 23
Extreme Fixes for Orthopedic Extremity Surgery
Print Shop: Insights on Orthopedic Additive Manufacturing
Molding Is Taking Its Place in Orthopedic Device Manufacturing
A View of Mixed-Reality Tech's Future in Orthopedics
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Exploring the Evolution and Future Trends of the Arthroscope Device Market
Designing for Terminal Sterilization Versus Re-Sterilization
Best Preparation Practices for Medical Emergencies in Orthopedic Manufacturing Facilities
How Medtech Can Transform Post-Surgical Outcomes in the US
Exploring 3DP/AM in the Healthcare Horizon
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Search Results for '
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Biologics
Preclinical Study Shows Biologic Effectively Promotes Bone Formation
Results will help Bone Biologics advance its rhNELL-1 growth factor into clinical trials.
Business Wire
01.28.20
Spine/Neurology
Bone Biologics Receives Human Research Ethics Committee OK for Clinical Trial
Company gets approval for the first center of a multicenter pilot clinical trial to evaluate NB1 (NELL-1/DBX) in Australia.
Business Wire
05.13.19
Spine/Neurology
FDA Approves Medtronic's Infuse Bone Graft for Use with PEEK Spine Implants
The approval adds two additional implants to current spine labeling.
GlobeNewswire
04.30.18
Xtant Medical Receives 510k Clearance for Expanded Indications of Irix-A
Irix-A is a standalone interbody device used in anterior lumber interbody fusions.
Globe Newswire
09.12.17
3-D Printing/Additive Mfg.
|
MIS/Robotics
|
Spine/Neurology
FDA Clears Camber Spine Technologies' 3D Printed SPIRA Open Matrix ALIF
510(k) clearance marks Camber's tenth spinal product to market.
PR Newswire
08.15.17
10. Globus Medical
...
08.15.17
Xtant Medical Receives FDA Clearance for the Xsert Lumbar Expandable Interbody System
Company expects to release product in mid-2017.
Xtant Medical Holdings Inc.
11.28.16
Spine/Neurology
SeaSpine Introduces Hollywood VI NanoMetalene Interbody Device
NanoMetalene-coated device combines benefits of titanium and PEEK in one spinal TLIF implant.
SeaSpine
06.16.16
FDA Clears Interventional Spine's Lordotic Opticage
Device is indicated for use with autogenous bone graft in patients with degenerative disc disease.
PR Newswire
05.27.16
Spine/Neurology
FDA Clears FORZA PTC Interbody Spacer System From Orthofix
Product is designed to restore normal disc height in patients suffering from degenerative disc disease.
Orthofix International N.V.
05.19.16
Amendia Launches the OmegaLIF Expandable Interbody Cage
Device is the first of several product launches the company plans for 2016.
Amendia Inc.
02.04.16
Breaking News
Siemens Healthineers Gains FDA Clearance for MAGNETOM Terra.X
AAOS Announces Research Funding for Orthopedic Specialty Societies
OssDsign Releases Encouraging TOP FUSION Study Data
Stryker Launches Gamma4 Hip Fracture Nailing System in Europe
Pathkeeper Surgical, Mayo Clinic Team Up on Pediatric Spine Surgery
View Breaking News >
CURRENT ISSUE
March/April 2024
Extreme Fixes for Orthopedic Extremity Surgery
Print Shop: Insights on Orthopedic Additive Manufacturing
Molding Is Taking Its Place in Orthopedic Device Manufacturing
A View of Mixed-Reality Tech's Future in Orthopedics
Improving Patient-Specific Outcomes with In-Silico Trials
View More >