DYNALOK PLUS™ Spinal System

GUDID 00673978973036

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

Primary Device ID	00673978973036
NIH Device Record Key	7c09bda8-d16d-479a-9a3e-e4ba7d0ce78a
Commercial Distribution Discontinuation	2018-10-08
Commercial Distribution Status	Not in Commercial Distribution
Brand Name	DYNALOK PLUS™ Spinal System
Version Model Number	8436072C
Company DUNS	830350380
Company Name	MEDTRONIC SOFAMOR DANEK, 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	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	00673978973036 [Primary]

MNH	Orthosis, spondylolisthesis spinal fixation

Steralize Prior To Use	true
Device Is Sterile	false

[00673978973036]

Moist Heat or Steam Sterilization

[00673978973036]

Moist Heat or Steam Sterilization