Rotation Medical Receives FDA 510(k) Clearance for Implantable Collagen Scaffold Technology

Rotation Medical announced that it has received 510(k) clearance from the U.S. Food and Drug Administration for its implantable collagen scaffold technology.

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The new technology is intended for use during arthroscopic and mini-open procedures to treat rotator cuff tears.

 

The company is also planning to conduct clinical studies to further demonstrate the effectiveness of the technology.

 

Rotation Medical is a medical device company focused on developing new technologies to treat rotator cuff disease.

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