TRIO TRAUMA 47110660

GUDID 04546540683182

CANNULATED SCREW

Stryker Corporation

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

Primary Device ID	04546540683182
NIH Device Record Key	68af7fb5-03ef-4dc9-bb98-6551dbdef7b8
Commercial Distribution Status	In Commercial Distribution
Brand Name	TRIO TRAUMA
Version Model Number	47110660
Catalog Number	47110660
Company DUNS	149183167
Company Name	Stryker 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	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	true
OTC Over-The-Counter	false

Device Dimensions

Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0
Length	60 Millimeter
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540683182 [Primary]

FDA Product Code

MNI	ORTHOSIS, SPINAL PEDICLE FIXATION