ConforMIS Receives FDA Approval for iTotal Patient-Specific Total Knee Replacement System

ConforMIS has received FDA 510(k) clearance for the patient-specific iTotal CR knee replacement system, according to a company news release.

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The iTotal CR is the first and only true patient-specific total knee replacement system commercially available. The patient-specific process customizes implants for each patient using CT scans from the patient’s knee. The image guides the proprietary design and manufacturing of the jigs and personalized implants for the patient.

The personalized software is designed to generate medial and lateral articulating surface geometries for each patient to mimic the patient’s natural anatomy.

Read more coverage on ConforMIS:

– ConforMIS Releases Second Generation of Knee Resurfacing System

– 10 Points on Personalized Knee Replacements

– ConforMIS Receives CE Mark for Its iUni G2 Patient-Specific Knee Replacement System

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