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ConforMIS Receives FDA 510(k) Clearance for New Hip Replacement System

June 23, 2017

ConforMIS, Inc. has won FDA 510(k) clearance for their iTotal Hip replacement system.  

The hip replacement system is based on patient specific-technology, using single-use 3D printed instruments, with an implementation system that requires little reusable instruments.

Previously, ConforMIS used their patient-specific methods to customize and replace knee implants. This FDA clearance allows an expansion of this system for other joint replacement procedures and encourages a growing trend in personalized treatments.

This product is aimed for a limited launch in 2019.

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