FDA Accepts Empirical Spine’s Limiflex PMA Module II
The LimiFlex DST is a first-of-its-kind surgical option for grade 1 degenerative spondylolisthesis patients with spinal stenosis. Jul 13, 2022
AlloSource Expands AlloConnex Line
Theh company added a quadricep tendon to its AlloConnex line of tendons, ligaments and fascia. Jul 13, 2022
Orthox to Commence Trial of FibroFix Knee Cartilage Repair
Orthox received permission in the UK to begin the "FFLEX Study" (derived from the "FibroFix cartiLage repair Experience"). Jul 13, 2022
Centinel Spine Gains FDA Approval for Additional prodisc Devices
Centinel Spine now has four PMA-approved cervical total disc replacement devices. Jul 13, 2022
Aurora Spine Announces New FDA indication clearance of Lumbar Spinal Stenosis for its ZIP™ series of MIS implants
FDA has cleared a new Lumbar Spinal Stenosis Indication for Aurora Spine's ZIP family of minimally invasive spinal implants. Jul 13, 2022
Bioventus Completes CartiHeal Acquisition
The addition of CartiHeal will complement the company's joint preservation technologies and specifically its HA business. Jul 12, 2022
3D-Side Closes €2.7 Million Series C Investment Round
Funds will support the positioning of company in the field of joint replacement, and launch of technologies in the U.S. Jul 12, 2022
Positive Policy Decision for ZimVie’s Anterior Vertebral Body Tethering
ZimVie's Tether device is now considered “medically necessary” for treatment of pediatric scoliosis, according to Anthem Blue Cross Blue Shield. Jul 12, 2022
Study Update: NEXXT MATRIXX 3-D Printed Technologies
Nexxt Spine completed enrollment and 6-month clinical data collection comparing NEXXT MATRIXX 3-D Printed titanium interbodies to PEEK devices. Jul 12, 2022
Enovis Completes Acquisition of Insight Medical Systems
The transaction expands the enabling technologies platform for Enovis'’ reconstructive portfolio with augmented reality surgical guidance. Jul 11, 2022
