Vu LPOD™ 12-TA-3016

GUDID 10889981039196

Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile

Primary Device ID	10889981039196
NIH Device Record Key	67de7a80-4891-447e-a3de-f73b650b74ad
Commercial Distribution Discontinuation	2016-09-02
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	Vu LPOD™
Version Model Number	12-TA-3016
Catalog Number	12-TA-3016
Company DUNS	079840876
Company Name	SEASPINE ORTHOPEDICS CORPORATION
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	false
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 Size Text, specify	0
Device Size Text, specify	0

Device Issuing Agency	Device ID
GS1	10889981039196 [Primary]

MAX	Intervertebral fusion device with bone graft, lumbar

Steralize Prior To Use	true
Device Is Sterile	false

[10889981039196]

Moist Heat or Steam Sterilization

[10889981039196]

Moist Heat or Steam Sterilization