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FDA 510(k), K110327, LDR SPINE ROI-A INTERBODY FUSION SYSTEM
FDA 510(k), K110327, LDR SPINE ROI-A INTERBODY FUSION SYSTEM
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510(K) Number: K110327
Device Name: LDR SPINE ROI-A INTERBODY FUSION SYSTEM
Manufacturer: LDR SPINE USA
Device Classification Name: intervertebral fusion device with integrated fixation, lumbar
Regulation Number: 888.3080
Classification Product Code: OVD
Date Received: 02/03/2011
Decision Date: 09/30/2011
Regulation Medical Specialty: Orthopedic
Device Name: LDR SPINE ROI-A INTERBODY FUSION SYSTEM
Manufacturer: LDR SPINE USA
Device Classification Name: intervertebral fusion device with integrated fixation, lumbar
Regulation Number: 888.3080
Classification Product Code: OVD
Date Received: 02/03/2011
Decision Date: 09/30/2011
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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