DUALX LLIF LOCKOUT SCREW 40MM

GUDID B707128300080010

Metallic spinal interbody fusion cage

Primary Device ID	B707128300080010
NIH Device Record Key	af075488-28f1-4114-af1d-7f207fa6c96c
Commercial Distribution Status	In Commercial Distribution
Brand Name	DUALX LLIF LOCKOUT SCREW 40MM
Version Model Number	12830008001
Company DUNS	081021000
Company Name	AMPLIFY SURGICAL, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
HIBCC	B707128300080010 [Primary]

MAX	Intervertebral Fusion Device With Bone Graft, Lumbar

Steralize Prior To Use	false
Device Is Sterile	true

B70712830008001A0	DUALX LLIF LOCKOUT SCREW 40MM
B707128300080010	DUALX LLIF LOCKOUT SCREW 40MM