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Home » Shoulder Innovations Gets 510(k) Clearance for Arthroplasty System
Shoulder Innovations Gets 510(k) Clearance for Arthroplasty System
![ClearanceStamp_Gray.gif](https://www.fdanews.com/ext/resources/test/Device_Images6/ClearanceStamp_Gray.gif?t=1576043982&width=430)
August 25, 2021
Holland, Mich.-based Shoulder Innovations has received 510(k) clearance from the FDA for its InSet reverse shoulder replacement system.
The InSet system includes artificial intelligence-based 3D preview software that helps clinicians with precise placement of the implant.
The system, which includes a range of implant types, was designed to simplify surgical procedures, potentially reducing complications and increase implant longevity, the company says.
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