FDA 510(k), K180220, SAGICO OSI Spinal System by Osimplant
FDA 510(k), K180220, SAGICO OSI Spinal System by Osimplant
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510(K) Number: K180220
Device Name: SAGICO OSI Spinal System by Osimplant
Manufacturer: Spinal Analytics & Geometrical Implant Co, LLC
Device Classification Name: Thoracolumbosacral Pedicle Screw System
Regulation Number: 888.3070
Classification Product Code: NKB
Date Received: 01/25/2018
Decision Date: 05/21/2018
Regulation Medical Specialty: Orthopedic
Device Name: SAGICO OSI Spinal System by Osimplant
Manufacturer: Spinal Analytics & Geometrical Implant Co, LLC
Device Classification Name: Thoracolumbosacral Pedicle Screw System
Regulation Number: 888.3070
Classification Product Code: NKB
Date Received: 01/25/2018
Decision Date: 05/21/2018
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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