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

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