
Acclarent, Inc.
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RELIEVA STRATUS PRO MICROFLOW SPACER (FRONTAL) is an FDA 510(k)-cleared medical device (K110687) 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 October 6, 2011. Regulation: 8.