KIT DUALX PLIF 0 DEG x 7-9MM

GUDID B70712823000001A0

Metallic spinal fusion cage, sterile

Primary Device ID	B70712823000001A0
NIH Device Record Key	ceaee67f-c815-474d-bc1c-d3f2bb8bffba
Commercial Distribution Status	In Commercial Distribution
Brand Name	KIT DUALX PLIF 0 DEG x 7-9MM
Version Model Number	12823000001A
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	B70712823000001A0 [Primary]

MAX	Intervertebral Fusion Device With Bone Graft, Lumbar

Steralize Prior To Use	false
Device Is Sterile	true

B70712823000001A0	Lordosis & Heights: 0° x 7-9mm Lateral Width: 21.1 mm Superior - Inferior Height: 9.5mm Anteri
B707128230000010	Lordosis & Heights: 0° x 7-9mm Collapsed Width (mm): 12.32 Expanded Width (mm): 21.1 Collapsed
B707128220000010	Lordosis & Heights: 0° x 7-9mm Collapsed Width (mm): 12.32 Expanded Width (mm): 21.1 Collapsed