
Stryker
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Stryker 90-S Max SERFAS Energy Probe is an FDA 510(k)-cleared medical device (K171391) manufactured by Stryker. 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 25, 2018. Regulation: 8.