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FDA 510(k), K083894, ALIF SPINAL TRUSS INTERBODY FUSION DEVICE
FDA 510(k), K083894, ALIF SPINAL TRUSS INTERBODY FUSION DEVICE
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510(K) Number: K083894
Device Name: ALIF SPINAL TRUSS INTERBODY FUSION DEVICE
Manufacturer: 4-WEB SPINE, LLC
Device Classification Name: intervertebral fusion device with bone graft, lumbar
Regulation Number: 888.3080
Classification Product Code: MAX
Date Received: 12/29/2008
Decision Date: 01/18/2011
Regulation Medical Specialty: Orthopedic
Device Name: ALIF SPINAL TRUSS INTERBODY FUSION DEVICE
Manufacturer: 4-WEB SPINE, LLC
Device Classification Name: intervertebral fusion device with bone graft, lumbar
Regulation Number: 888.3080
Classification Product Code: MAX
Date Received: 12/29/2008
Decision Date: 01/18/2011
Regulation Medical Specialty: Orthopedic
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- 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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