FDA 510(k), K100820, WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEM

FDA 510(k), K100820, WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEM

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510(K) Number: K100820
Device Name: WENZEL SPINE VARILIFT INTERBODY FUSION SYSTEM
Manufacturer: WENZEL SPINE
Device Classification Name: intervertebral fusion device with bone graft, lumbar
Regulation Number: 888.3080
Classification Product Code: MAX
Date Received: 03/23/2010
Decision Date: 08/05/2010
Regulation Medical Specialty: Orthopedic

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