InFIll Lateral Parallel

GUDID 00814729024670

Interspinous spinal fixation implant

Primary Device ID	00814729024670
NIH Device Record Key	8185dedb-d9ed-4b61-81a9-da5f9971396c
Commercial Distribution Status	In Commercial Distribution
Brand Name	InFIll Lateral Parallel
Version Model Number	53-6010
Company DUNS	962347980
Company Name	PINNACLE SPINE GROUP, LLC
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	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00814729024670 [Primary]

MAX	Intervertebral Fusion Device With Bone Graft, Lumbar

Steralize Prior To Use	true
Device Is Sterile	true

[00814729024670]

Radiation Sterilization;Moist Heat or Steam Sterilization

[00814729024670]

Radiation Sterilization;Moist Heat or Steam Sterilization