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
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
- 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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