Nextremity Solutions Gains FDA Clearance for Metatarsophalangeal Joint Arthrodesis System
The continued expansion of Nextremity Solutions' portfolio addresses additional complications in the foot.
Regulatory
Articles
Gramercy Extremity Orthopedics Gains FDA Clearance for GEO FirstFuse MTPJ Fusion Plate
Gramercy Extremity Orthopedics was granted FDA 510(k) clearance for the GEO FirstFuse MTPJ Fusion Plate.
OSSIO Gains FDA Clearance for OSSIOfiber Hammertoe Fixation
OSSIO was granted FDA 510(k) clearance to market the OSSIOfiber® Hammertoe Fixation system.
Paragon 28 Gains FDA Clearance for Phantom ActivCore Nail
Paragon 28 was granted FDA 510(k) clearance to market the Phantom® ActivCore Nail.
Silver Bullet Therapeutics Gains CE Mark for OrthoFuzIon Bone Screw
Silver Bullet Therapeutics received CE Mark approval for the OrthoFuzIon™ Bone Screw for reduction and internal fixation procedures anywhere in the body.
Nextremity Solutions Gains Clearance for Lesser TMT Joint Arthrodesis System
Nextremity Solutions received FDA 510(k) clearance to market the InCore® TMT system, a three-part construct for fixation for Lesser Tarsometatarsal Joint Arthrodesis.
U.K.’s NICE Maintains Recommendation for Bioventus’ EXOGEN
The National Institute for Health and Clinical Excellence in the U.K. updated its guidance regarding use of Bioventus' EXOGEN® Ultrasound Bone Healing System to treat long bone fractures.
Active Implants Receives FDA Breakthrough Device Designation for NUsurface Meniscus Implant
Active Implants was granted a Breakthrough Device Designation from FDA for the NUsurface® Meniscus Implant. If cleared by FDA, NUsurface would be the first artificial meniscus in the U.S. market.
The Orthopaedic Implant Company in Pilot Program to Lower Supply Costs
The Orthopaedic Implant Company is participating in a pilot program which has led to a $3.6MM reduction in supply expenses for one integrated delivery network.
Stryker Unsuccessful in KFx Medical Patent Challenge
The U.S. Patent Trial and Appeal Board denied Stryker's request for an inter partes review of challenged claims in a suit pertaining to KFx Medical's suture anchors.