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![APEX KNEE SYSTEM, MODEL KC-230XY, KC-240XY [ NO HOLES, 2 HOLES] — view 1](/_next/image?url=https%3A%2F%2Fimages.pexels.com%2Fphotos%2F8160583%2Fpexels-photo-8160583.jpeg%3Fauto%3Dcompress%26cs%3Dtinysrgb%26w%3D600&w=3840&q=75)
Omni Life Science, Inc.
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APEX KNEE SYSTEM, MODEL KC-230XY, KC-240XY [ NO HOLES, 2 HOLES] is an FDA 510(k)-cleared medical device (K080842) manufactured by Omni Life Science, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 22, 2008. Regulation: 8.