Linvatec Corp.
RESECTION ABLATOR
SKU K013369UPC GEI
In Stock
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IIFDA 510(k) Cleared (K013369)
1
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Linvatec Corp.
Free shipping on orders over $99 · 30-day returns
RESECTION ABLATOR is an FDA 510(k)-cleared medical device (K013369) manufactured by Linvatec Corp.. 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 3, 2002. Regulation: 8.
