Home » CartiHeal Nabs FDA Breakthrough Device Designation for Cartilage Lesion Implant
CartiHeal Nabs FDA Breakthrough Device Designation for Cartilage Lesion Implant
The FDA has granted a Breakthrough Device designation for CartiHeal’s Agili-C implant, a device used to treat cartilage lesions in joints.
The implant is used to treat cartilage lesions in both arthritic and nonarthritic joints. Cartilage lesions can be caused by a number of different injuries, including falling and athletic incidents, and are characterized by aching pain, swelling, impaired function and pain during activities.
The company is currently conducting a pivotal investigational device exemption (IDE) trial evaluating the implant’s superiority over current surgical standard of care, microfracture and debridement; 251 participants have been enrolled.
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