Zimmer Biomet Gains CE Mark for Persona Revision Knee
Persona Revision offers a personalized fit and optimized function for patients undergoing revision knee surgery. Nov 18, 2024
THINK Surgical Gains 510(k) for LinkSymphoKnee Implants with TMINI
LinkSymphoKnee is added to THINK Surgical's ID-HUB data bank of implant modules for use with the open platform version of its TMINI System in the U.S. Nov 18, 2024
Locate Bio Launches LDGraft RESTORE Study
LDGraft is a combination product that delivers recombinant human bone morphogenetic protein-2 through a biodegradable polymer. Nov 18, 2024
Study Demonstrates Advantages of Nevro1 SI Joint Fusion
Nevro1 is an FDA 510(k)-cleared device intended to transfix the SI joint for immediate stability and long-term fusion. Nov 18, 2024
Osteal Therapeutics Reports Positive Study Results
Two prospective, randomized, comparative studies evaluated the efficacy of a rapid exchange arthroplasty with intra-articular antibiotic irrigation vs. two-stage exchange arthroplasty. Nov 18, 2024
OSSIO Launches OSSIOfiber Threaded Trimmable Fixation Nail
Use cases for the system include hand and wrist, foot and ankle, sports medicine and pediatric applications. Nov 14, 2024
Expanded Positive Coverage for Centinel Spine’s prodisc L
With these positive coverage updates, it is estimated that one-level lumbar TDR coverage is nearly 95% of the commercially-covered lives in the U.S. Nov 14, 2024
NovaBone Putty Cleared for Use in Interbody Fusion
The FDA clearance allows NovaBone Putty to be used in the intervertebral disc space alongside FDA-cleared interbody fusion devices. Nov 13, 2024
Acuitive Technologies Gains 510(k) for CITREPORE Bone Void Filler
CITREPORE is a synthetic bioactive bone void filler composed of patented CITREGEN biomaterial technology. Nov 12, 2024
Foundation Surgical Unveils Motion Preservation Procedure with 510(k) Clearance
Vertiwedge is the first intraosseous device designed to facilitate and maintain vertebral body correction of partially collapsed vertebrae. Nov 08, 2024
