
Stryker Instruments
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STRYKER CONSOLIDATED OPERATING ROOM EQUIPMENT (CORE) SYSTEM is an FDA 510(k)-cleared medical device (K032303) manufactured by Stryker Instruments. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 15, 2004. Regulation: 8.