TRIO TRAUMA 47110835

GUDID 04546540683236

CANNULATED SCREW

Stryker Corporation

Bone-screw internal spinal fixation system, non-sterile

Primary Device ID	04546540683236
NIH Device Record Key	e108bc96-28f1-4f60-bcf2-a338d0006be7
Commercial Distribution Status	In Commercial Distribution
Brand Name	TRIO TRAUMA
Version Model Number	47110835
Catalog Number	47110835
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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540683236 [Primary]

FDA Product Code

MNI	ORTHOSIS, SPINAL PEDICLE FIXATION