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Home » Shoulder Innovations’ Humeral System Cleared by FDA
Shoulder Innovations’ Humeral System Cleared by FDA
![ClearanceStamp_Gray.gif](https://www.fdanews.com/ext/resources/test/Device_Images6/ClearanceStamp_Gray.gif?t=1576043982&width=430)
November 5, 2018
The FDA granted 510(k) clearance to Shoulder Innovations’ InSet humeral short stem system for use in shoulder arthroplasty.
The system includes products used in partial or total shoulder arthroplasty, a surgical procedure that uses a prosthetic implant to treat degenerative, rheumatoid or traumatic arthritis in the shoulder.
InSet includes coating technology for implant fixation while preserving the humerus bone.
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