The FDA has granted approval for a supplemental Biologics License Application, allowing for the arthroscopic delivery of MACI (autologous cultured chondrocytes on porcine collagen membrane) in the repair of knee cartilage defects. This approval provides a less invasive option for surgeons and patients seeking to address symptomatic, full-thickness cartilage damage.
MACI Arthro: A Less Invasive Approach
Vericel Corporation, the manufacturer of MACI, announced that the approval covers the arthroscopic delivery of MACI to repair single or multiple full-thickness cartilage defects of the knee, up to 4 cm2 in size. MACI is an autologous cellularized scaffold product, utilizing tissue engineering to grow cells on scaffolds using healthy cartilage tissue harvested from the patient's own knee.
According to Vericel, MACI Arthro allows surgeons to evaluate and prepare the defect site and deliver the MACI implant through small incisions using custom-designed instruments. This contrasts with the existing method of administration, offering a less invasive technique.
Impact and Market Potential
Nick Colangelo, CEO of Vericel, stated, "The approval of MACI Arthro represents another significant milestone in our strategy to provide innovative solutions for patients suffering from pain and dysfunction caused by cartilage defects in the knee." He added that MACI Arthro has the potential to significantly increase penetration into the largest segment of the MACI addressable market and will support sustained top-tier revenue growth for the company in the years ahead.
MACI Arthro stands out as the only restorative biologic cartilage repair product currently approved for arthroscopic administration.