Harrier SA

GUDID 00840996177245

Intervertebral-body internal spinal fixation system

Primary Device ID	00840996177245
NIH Device Record Key	d3ee0ad4-626c-48fc-9500-3fd8f51e2e3e
Commercial Distribution Status	In Commercial Distribution
Brand Name	Harrier SA
Version Model Number	Y070-26321008
Company DUNS	078293017
Company Name	Choice Spine, LP
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	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 Issuing Agency	Device ID
GS1	00840996177245 [Primary]

MAX	Intervertebral fusion device with bone graft, lumbar

Steralize Prior To Use	true
Device Is Sterile	false

[00840996177245]

Moist Heat or Steam Sterilization

00840996177245	Harrier SA 26x32x8, 10 Deg
00840996177238	28x36x10,10deg Trial
00840996177221	28x36x8,10deg Trial
00840996184052	HARRIER-SA,SCREW,5.5X40
00840996184045	HARRIER-SA,SCREW,5.5X35
00840996184038	HARRIER-SA,SCREW,5.5X30
00840996184021	HARRIER-SA,SCREW,5.5X25
00840996184014	HARRIER-SA,SCREW,5.5X20
00840996184007	HARRIER-SA,SCREW,5.0x35
00840996183994	HARRIER-SA,SCREW,5.0x40
00840996183987	HARRIER-SA,SCREW,5.0x30
00840996183970	HARRIER-SA,SCREW,5.0x25
00840996183963	HARRIER-SA,SCREW,5.0x20
00840996192965	HARRIER-SA,TRIAL,START WEDGE IMPACT 6H
00840996192958	HARRIER-SA,TRIAL,START WEDGE IMPACT 8H