The US FDA Grants 510(k) Clearance to Zimmer Biomet’s Persona Revision SoluTion Femur
Shots:
- The US FDA has granted 510(k) clearance to Persona Revision SoluTion Femur as an alternative for knee implant in pts with metal sensitivities; commercially available in the US in Q3’25
- SoluTion Femur, part of the Persona Revision Knee System, utilizes surface-hardening treatment for enhanced wear performance & provides surgeons with anatomic components, incl. tibial as well as femoral cones & various stem choices for zonal fixation
- SoluTion Femur is made from Tivanium (Ti-6Al-4V) alloy with Ti-Nidium surface hardening for enhanced strength & is available in standard as well as plus sizes to improve flexion instability & soft tissue balancing, while reducing implant overhang
Ref: Prnewswire | Image: Zimmer Biomet
Related News:- Zimmer Biomet to Acquire Paragon 28 for ~$1.2B
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Ridhi is an avid secondary researcher who follows trends in the biopharmaceutical and healthcare sectors to curate engaging content for the global audience. She works as a news editor at PharmaShots and loves to read books and explore new destinations.
