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...
Active Implants was granted a Breakthrough Device Designation from FDA for the NUsurface® Meniscus Implant. If cleared by FDA, NUsurface would be...
OrthoSpin received FDA 510(k) clearance to market its smart robotic external fixator....
The U.S. Patent Trial and Appeal Board denied Stryker's request for an inter partes review of challenged claims in a suit pertaining...
Zimmer Biomet was granted FDA 510(k) clearance for the JuggerStitch device for meniscal repair....
Orthoscan launched the TAU family of mini C-arms, designed and approved for use with pediatric patients....
Preliminary study results indicate that X-BOLT Orthopaedics' X-BOLT device for hip fracture repair demonstrated a cut-out rate of 0.8% in...
Fuse Medical grew their sports medicine offerings with Galen Medial and Galen XT Suture Anchors, the Kopis Knotless Anchor and Vida...
OrthoPediatrics launched next-generation Cannulated Screw systems in the U.S. to treat pediatric fractures and fusions....
CoNextions Medical completed enrollment in the clinical trial of the CoNextions TR tendon-to-tendon repair device....
Smith & Nephew launched the EVOS WRIST Plating System to treat simple and complex wrist fractures....
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