TECHTONIX 6262550

GUDID 07613154108893

SCREW

Stryker Corporation

Bone-screw internal spinal fixation system, non-sterile

Primary Device ID	07613154108893
NIH Device Record Key	34c99150-1793-4b17-83aa-2812af46e9fd
Commercial Distribution Status	In Commercial Distribution
Brand Name	TECHTONIX
Version Model Number	6262550
Catalog Number	6262550
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	07613154108893 [Primary]

FDA Product Code

KWP	APPLIANCE, FIXATION, SPINAL INTERLAMINAL