TECHTONIX 6262560

GUDID 07613327066708

SCREW

Stryker Corporation

Bone-screw internal spinal fixation system, non-sterile

Primary Device ID	07613327066708
NIH Device Record Key	d73245a6-68eb-4742-ba34-e2d99a8be9fb
Commercial Distribution Status	In Commercial Distribution
Brand Name	TECHTONIX
Version Model Number	6262560
Catalog Number	6262560
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
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Length	60 Millimeter
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Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327066708 [Primary]

FDA Product Code

KWP	APPLIANCE, FIXATION, SPINAL INTERLAMINAL