FDA Grants Cytori 510(k) Clearance for Puregraft 850

Cytori

has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for the Puregraft(R) 850 System for body contouring using a patient's own fat. The Puregraft(R) 850 product line extension provides optimized and sterile processing of up to 850 mL of tissue, a significantly larger volume than the Puregraft(R) 250, which received a 510(k) in January 2010. Larger tissue volumes expand the range of soft tissue procedures for which the product line may be used.