Zimmer Biomet Receives FDA 510(k) Clearance for Unite3D Bridge Fixation System
Zimmer Biomet received FDA 510(k) clearance for the Unite3D™ Bridge Fixation System, 3D-printed technology designed for use in foot and ankle...
Zimmer Biomet received FDA 510(k) clearance for the Unite3D™ Bridge Fixation System, 3D-printed technology designed for use in foot and ankle...
MX Orthopedics received FDA 510(k) clearance to market the dynaMX™ Compression Staple, a superelastic Nitinol-based device. ...
Tyber Medical commenced full market launch of its TyWedge™ Osteotomy Wedge System, featuring TyPEEK® proprietary titanium plasma-sprayed PEEK coating specifically indicated for...
Merete Technologies launched PediatrOS™ RigidTack™/FlexTack™ novel epiphysiodesis staples. ...
The Orthopaedic Implant Company launched its Intramedullary Hip Nail....
Bio2 Technologies received FDA 510(k) clearance to market a fusion system for interphalangeal fusion, fracture repair and osteotomies of toes,...
Agent Medical launched ArthroBridgeâ„¢, an implant for the treatment of hammertoes, and the ArthroMateâ„¢ rasp designed for rear foot fusion...
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