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FDA 510(k), K092011, NORM SPINAL SYSTEM
FDA 510(k), K092011, NORM SPINAL SYSTEM
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510(K) Number: K092011
Device Name: NORM SPINAL SYSTEM
Manufacturer: NORM TIBBI URUNLER ITHALAT IHRACAT SANAYI VE TICAR
Device Classification Name: Orthosis, Spondylolisthesis Spinal Fixation
Regulation Number: 888.3070
Classification Product Code: MNH
Date Received: 07/06/2009
Decision Date: 10/28/2009
Regulation Medical Specialty: Orthopedic
Device Name: NORM SPINAL SYSTEM
Manufacturer: NORM TIBBI URUNLER ITHALAT IHRACAT SANAYI VE TICAR
Device Classification Name: Orthosis, Spondylolisthesis Spinal Fixation
Regulation Number: 888.3070
Classification Product Code: MNH
Date Received: 07/06/2009
Decision Date: 10/28/2009
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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