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Stryker Spine
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LITE DECOMPRESSION SYSTEM- LIGHT CABLE MODEL 48089999 is an FDA 510(k)-cleared medical device (K122637) manufactured by Stryker Spine. 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 October 31, 2012. Regulation: 8.