
Stryker Corporation
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OptaBlate RF Generator, OptaBlate Probes, OptaBlate Microinfuser Infusion Device is an FDA 510(k)-cleared medical device (K221074) manufactured by Stryker Corporation. 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 September 15, 2022. Regulation: 8.