Duo Lumbar Interbody Fusion System 860-8007

GUDID M7408608007

Polymeric spinal fusion cage, sterile

Primary Device ID	M7408608007
NIH Device Record Key	6a525c18-3c5d-4bf3-833e-0364fd1dc523
Commercial Distribution Status	In Commercial Distribution
Brand Name	Duo Lumbar Interbody Fusion System
Version Model Number	86-08-17-14
Catalog Number	860-8007
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	info@spineology.com

Height

14 Millimeter

Device Issuing Agency	Device ID
HIBCC	M7408608007 [Primary]

MAX	Intervertebral fusion device with bone graft, lumbar

Steralize Prior To Use	true
Device Is Sterile	false

[M7408608007]

Moist Heat or Steam Sterilization