Vendor/Manufacturer: Stryker
Product/Product Line: SERRATO Screw
Vendor/Manufacturer Catalog #: 482616545
Global Unique Device (GUD) Primary Device Identifier Number: 07613327352658
Global Unique Device (GUD) Device Description:
Polyaxial Screw
Global Medical Device Nomenclature (GMDN) Preferred Term Name:
Bone-screw internal spinal fixation system, non-sterile
Category 1: Spine
Category 2: Lumbar Pedicle Screw Systems
Category 3: Screw
Category 4: Two Level
Quantity of "Each"es needed in each System/Set: 6
FDA Regulation Medical Specialty: Orthopedic Devices - Prosthetic Devices
FDA Regulation Number: 888.3070
FDA Regulation Description Classification Name:
Thoracolumbosacral pedicle screw system
FDA Classification Product Code: NKB
FDA Classification Product Code Device Name:
Thoracolumbosacral Pedicle Screw System
FDA Premarket Submissions: NA
SUBSTANTIALLY EQUIVALENT to the following products:
1. NA
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