Ceremed , Inc.
BIOPOR AOC POROUS POLYETHYLENE, CEREPOR
SKU K141880UPC KKY
In Stock
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IIFDA 510(k) Cleared (K141880)
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Free shipping on orders over $99 · 30-day returns
Ceremed , Inc.
Free shipping on orders over $99 · 30-day returns
BIOPOR AOC POROUS POLYETHYLENE, CEREPOR is an FDA 510(k)-cleared medical device (K141880) manufactured by Ceremed , 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 April 15, 2015. Regulation: 8.
