Duo Lumbar Interbody Fusion System 100-1030

GUDID M7401001030

Polymeric spinal fusion cage, sterile

Primary Device ID	M7401001030
NIH Device Record Key	3da07e53-a0e2-4a9e-980b-8c6e83c9e14e
Commercial Distribution Status	In Commercial Distribution
Brand Name	Duo Lumbar Interbody Fusion System
Version Model Number	101-56-02-16
Catalog Number	100-1030
Company DUNS	033014361
Company Name	SPINEOLOGY INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	MR Unsafe
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Phone	+1(651)256-8500
Email	aadams@spineology.com

Height	16 Millimeter
Height	16 Millimeter

Device Issuing Agency	Device ID
HIBCC	M7401001030 [Primary]

MAX	Intervertebral fusion device with bone graft, lumbar

Steralize Prior To Use	true
Device Is Sterile	false

[M7401001030]

Moist Heat or Steam Sterilization