Ceremed , Inc.
AOC POROUS POLYETHYLENE, AOC POROUS HDPE, AOC POROUS POLYETHYLENE SURGICAL IMPLANT, CEREPOR
SKU K043133UPC KKY
In Stock
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IIFDA 510(k) Cleared (K043133)
1
Free shipping on orders over $99 · 30-day returns
Ceremed , Inc.
Free shipping on orders over $99 · 30-day returns
AOC POROUS POLYETHYLENE, AOC POROUS HDPE, AOC POROUS POLYETHYLENE SURGICAL IMPLANT, CEREPOR is an FDA 510(k)-cleared medical device (K043133) 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 March 1, 2005. Regulation: 8.
