Amplitude Surgical Files for ANATOMIC Knee 510(k)
Amplitude Surgical filed for FDA 510(k) clearance of its posterior stabilized ANATOMIC® knee prosthesis....
Jun 09, 2016,
Joint Replacement
ORTHOFLASHIntegra LifeSciences Launches Fin-Lock™ Glenoid
Integra LifeSciences launched the Integra® Fin-Lock™ Glenoid for the Titan™ Modular Shoulder System to address glenoid component loosening and failure in total shoulder...
May 24, 2016,
Medacta Reports on Device Utilization
Results from a 421-patient study revealed a 97.75% survival rate at 5 years for Medacta’s AMIStem hip implant. AMIStem has been implanted >100,000 times,...
May 19, 2016,
Results from Study of Moximed’s Atlas Knee
Study results suggest that Moximed’s Atlas™ knee provided rapid, clinically-effective pain relief for patients with early knee OA in the pre-arthroplasty disease...
May 09, 2016,
Stryker Performance Solutions Launches JointCOACH Program
Stryker Performance Solutions launched JointCOACH™, a digital engagement and education platform to coordinate care delivery and improve the experience of...
Apr 27, 2016,
Integra LifeSciences Announces Initial Clinical Use of Cadence Total Ankle in the U.S.
Integra LifeSciences announced successful completion of initial procedures using the Integra® Cadence™ Total Ankle....
Apr 26, 2016,
Exactech Receives FDA 510(k) Clearance for Vantage Total Ankle
Exactech received FDA 510(k) clearance to market the Vantage™ Total Ankle. Targeted clinical evaluation will commence in mid-2016, with full launch...
Apr 25, 2016,
Episurf Medical Receives Expanded Reimbursement Coverage in the EU
Episurf Medical’s Episealer® procedure received expanded reimbursement coverage in the U.K., Netherlands and Belgium. The patient-specific implants and Epiguide® drill guides are designed...
Apr 20, 2016,
Bodycad Introduces Bodycad OnCall Custom Orthopaedic Restorations
Bodycad introduced Bodycad OnCall™, personalized, individually-manufactured orthopaedic restorations for complex cases, particularly oncology, revision and osteotomy applications....
Apr 07, 2016,
ConforMIS Update on iTotal Hip FDA Submission
ConforMIS withdrew its FDA 510(k) application for the iTotal Hip device, and plans to submit a new application in 2H16....
Apr 04, 2016,
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