INTERBODY FUSION ALIF0826-15P

GUDID 00815362023129

Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage Polymeric spinal interbody fusion cage

Primary Device ID	00815362023129
NIH Device Record Key	5f08be17-d0d0-42a2-b2fd-ebb12ebb7888
Commercial Distribution Status	In Commercial Distribution
Brand Name	INTERBODY FUSION
Version Model Number	5120PM
Catalog Number	ALIF0826-15P
Company DUNS	079398589
Company Name	PRECISION SPINE, INC.
Device Count	1
DM Exempt	true
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	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00815362023129 [Primary]

MAX	Intervertebral Fusion Device With Bone Graft, Lumbar

Steralize Prior To Use	true
Device Is Sterile	false

[00815362023129]

Moist Heat or Steam Sterilization

[00815362023129]

Moist Heat or Steam Sterilization

[00815362023129]

Moist Heat or Steam Sterilization