FDA 510(k), K083475, LUCENT MAGNUM

FDA 510(k), K083475, LUCENT MAGNUM

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510(K) Number: K083475
Device Name: LUCENT MAGNUM
Manufacturer: SPINAL ELEMENTS, INC.
Device Classification Name: Intervertebral Fusion Device With Integrated Fixation, Lumbar
Regulation Number: 888.3080
Classification Product Code: OVD
Date Received: 11/24/2008
Decision Date: 02/13/2009
Regulation Medical Specialty: Orthopedic

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