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Rsb Spine, LLC
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INTERPLATE INTERBODY FUSION DEVICE, MODELS C, CGC, L AND LGC is an FDA 510(k)-cleared medical device (K071922) manufactured by Rsb Spine, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on September 17, 2007. Regulation: 8.