Acclarent, Inc.
MODIFICATION TO RELIEVA STRATUS MICROFLOW SPACER
SKU K093594UPC KAM
In Stock
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IFDA 510(k) Cleared (K093594)
1
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Acclarent, Inc.
Free shipping on orders over $99 · 30-day returns
MODIFICATION TO RELIEVA STRATUS MICROFLOW SPACER is an FDA 510(k)-cleared medical device (K093594) manufactured by Acclarent, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 2, 2010. Regulation: 8.
