NuVasive Gains Latest FDA 510(k) for Pulse Platform
NuVasive announced the commercial launch of Pulse, which is now available for sale in targeted global regions. Jul 30, 2021
ARVIS Augmented Reality Gains FDA 510(k) Clearance
ARVIS is the first wearable surgical navigation system to be cleared for both hip and knee arthroplasty. Jul 29, 2021
Medacta Expands Hip Revision Portfolio
First cases are complete using the AMIS-K Long, Iliac Screw Mpact 3D Metal and 3D Metal B-Cage, following CE Mark approval. Jul 29, 2021
First U.S. Cases with Orthofix fiberFUSE Strip Bone Graft
fiberFUSE Strip is formulated to enable optimized application for posterior cervical, posterior lumbar and degenerative spinal procedures. Jul 28, 2021
Carlsmed Partners to Study aprevo Spinal Device
The International Spine Study Group Foundation will help collect data on surgical treatment with the personalized interbody device. Jul 28, 2021
Study Results: Aesculap Implant Systems’ activL Artificial Disc
Patient outcomes at seven years post-op compare the activL Artificial Disc with the ProDisc-L to treat single-level lumbar degenerative disc disease. Jul 27, 2021
MiRus Raises $65 Million for Expansion of Rhenium-based Medical Devices
MiRus completed a highly oversubscribed funding round for growth of its spine and extremity portfolios and other solutions using Rhenium-based alloys (MoRe). Jul 27, 2021
NuVasive Launches Modulus ALIF Porous Implant for Anterior Spine Surgery
Modulus ALIF provides implants and instrumentation designed for both supine ALIF and XALIF procedures. Jul 22, 2021
European Study with 5-year Follow-up of Episealer Talus Patients
Episealer Talus is Episurf Medical’s CE Marked joint implant for treatment of osteochondral ankle lesions. Jul 22, 2021
Study Results: REGENETEN Bioinductive Implant in Rotator Cuff Tear
Investigators compared the REGENETEN Implant alone vs. with traditional surgical repair to treat partial-thickness rotator cuff tears. Jul 21, 2021
