Cytori Therapeutics, Inc.
PUREGRAFT 50 SYSTEM
SKU K132815UPC MUU
In Stock
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IIFDA 510(k) Cleared (K132815)
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Free shipping on orders over $99 · 30-day returns
Cytori Therapeutics, Inc.
Free shipping on orders over $99 · 30-day returns
PUREGRAFT 50 SYSTEM is an FDA 510(k)-cleared medical device (K132815) manufactured by Cytori Therapeutics, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 23, 2014. Regulation: 8.
