Implanet Granted CE Mark Renewal for Madison Knee
European authorities extended the CE Mark approvals on the entire range of MADISON knee devices for a further four years....
European authorities extended the CE Mark approvals on the entire range of MADISON knee devices for a further four years....
Rejoint offers more than 6,300 femoral variations including multiple designs and coatings. FDA 510(k) clearance is expected in 2Q21....
The patent is titled “System and method for creating a decision support material indicating damage to an anatomical joint.”...
Study results indicate that procedures using OXINIUM on XLPE had the lowest risk of revision of all bearing combinations for...
The two components allow surgeons to widen clinical use of the system by addressing more patient morphologies and pathologies....
Conformis and Zimmer Biomet settled disputes related to patient-specific instrument patents for use with off-the-shelf knee, hip and shoulder implants....
The patent covers Episurf Medical’s 3D-based damage marking technology, central to the Episealer® implant system....
The new system debuts a lateral-specific tibia baseplate and an increased size range for femoral components and medial tibia baseplates....
Medacta gained FDA clearance for its M-Vizion Femoral Revision System and its Long Humeral Diaphysis for shoulder joint replacement....
The risk stratification tool intends to help surgeons transition more total joint arthroplasty cases to outpatient or same-day discharge....
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