Smith & Nephew, Inc.
MODIFICATION TO SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE
SKU K071300UPC GXI
In Stock
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IIFDA 510(k) Cleared (K071300)
1
Free shipping on orders over $99 · 30-day returns
Smith & Nephew, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO SMITH & NEPHEW RF DENERVATION PROBES & RF CANNULAE is an FDA 510(k)-cleared medical device (K071300) manufactured by Smith & Nephew, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 19, 2007. Regulation: 8.
