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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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