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Depuy Synthes/EIT CONDUIT. Interbody Fusion Device. Lumbar/T-Lumbar. Non-Bone. Catalog #PUI80906


Vendor/Manufacturer: DePuy Synthes/EIT

Product/Product Line: CONDUIT Interbody Fusion Device

Vendor/Manufacturer Catalog #: PUI80906

Global Unique Device (GUD) Primary Device Identifier Number:

04260557779965

Global Unique Device (GUD) Device Description:

EIT PLIF, H 9mm, 8°, 26/9

Global Medical Device Nomenclature (GMDN) Preferred Term Name:

Metallic spinal interbody fusion cage

FDA Regulation Medical Specialty:

Orthopedic Devices - Prosthetic Devices

FDA Regulation Number: 888.3080

FDA Regulation Description Classification Name:

Intervertebral body fusion device

FDA Classification Product Code: MAX

FDA Classification Product Code Device Name:

Intervertebral Fusion Device With Bone Graft, Lumbar


Category 1: Spine

Category 2: Interbody Fusion Devices

Category 3: Lumbar/T-Lumbar

Category 4: Non-Bone


FDA Premarket Submissions: K170503


SUBSTANTIALLY EQUIVALENT to the following products:

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