Superion Indirect Decompression System 101-9814

GUDID 00884662000550

Lumbar interspinous decompression spacer, sterile

Primary Device ID	00884662000550
NIH Device Record Key	71368eff-ccef-4108-bb38-315e951b9964
Commercial Distribution Status	In Commercial Distribution
Brand Name	Superion Indirect Decompression System
Version Model Number	14mm
Catalog Number	101-9814
Company DUNS	005235436
Company Name	VERTIFLEX, INC.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	MR Conditional
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	false
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	00884662000550 [Primary]

NQO	Prosthesis, Spinous Process Spacer/Plate

Steralize Prior To Use	false
Device Is Sterile	true

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