FDA approves first autologous cellularized scaffold for the repair of cartilage defects of the knee

FDA

14 December 2016 - The U.S. FDA today approved Maci (autologous cultured chondrocytes on porcine collagen membrane) for the repair of symptomatic, full-thickness cartilage defects of the knee in adult patients. 

Maci is the first FDA-approved product that applies the process of tissue engineering to grow cells on scaffolds using healthy cartilage tissue from the patient’s own knee.

Read FDA press release

Michael Wonder

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Michael Wonder

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Outcome , US , Device