FDA 510(k), K140276, CD HORIZON SPINAL SYSTEM
FDA 510(k), K140276, CD HORIZON SPINAL SYSTEM
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510(K) Number: K140276
Device Name: CD HORIZON SPINAL SYSTEM
Manufacturer: MEDTRONIC SOFAMOR DANEK
Device Classification Name: pedicle screw spinal system, adolescent idiopathic scoliosis
Regulation Number: 888.3070
Classification Product Code: OSH
Date Received: 02/03/2014
Decision Date: 03/13/2014
Regulation Medical Specialty: Orthopedic
Device Name: CD HORIZON SPINAL SYSTEM
Manufacturer: MEDTRONIC SOFAMOR DANEK
Device Classification Name: pedicle screw spinal system, adolescent idiopathic scoliosis
Regulation Number: 888.3070
Classification Product Code: OSH
Date Received: 02/03/2014
Decision Date: 03/13/2014
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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