Arthrex, Inc.
ARTHREX FIBERTAPE (TM), 2MM, ARTHREX FIBERTAPE (TM), 3MM, ARTHREX FIBERTAPE (TM), 4MM, MODELS AR-7237, AR-7238, AR-7239
SKU K032245UPC GAT
In Stock
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IIFDA 510(k) Cleared (K032245)
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Free shipping on orders over $99 · 30-day returns
Arthrex, Inc.
Free shipping on orders over $99 · 30-day returns
ARTHREX FIBERTAPE (TM), 2MM, ARTHREX FIBERTAPE (TM), 3MM, ARTHREX FIBERTAPE (TM), 4MM, MODELS AR-7237, AR-7238, AR-7239 is an FDA 510(k)-cleared medical device (K032245) manufactured by Arthrex, 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 13, 2004. Regulation: 8.
