TECHTONIX 6262540

GUDID 04546540443809

SCREW

Stryker Corporation

Bone-screw internal spinal fixation system, non-sterile Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable Spinal bone screw, non-bioabsorbable

Primary Device ID	04546540443809
NIH Device Record Key	d3874ba5-86f2-4ad1-aab3-c911e2a9f691
Commercial Distribution Status	In Commercial Distribution
Brand Name	TECHTONIX
Version Model Number	6262540
Catalog Number	6262540
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	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Length	40 Millimeter
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Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540443809 [Primary]

FDA Product Code

KWP	APPLIANCE, FIXATION, SPINAL INTERLAMINAL