ASNIS 606150

GUDID 07613153051770

Cannulated Screw

Stryker Trauma SA

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

Primary Device ID	07613153051770
NIH Device Record Key	0d32ad0b-b417-483b-8bdc-59554d912992
Commercial Distribution Status	In Commercial Distribution
Brand Name	ASNIS
Version Model Number	606150
Catalog Number	606150
Company DUNS	481999654
Company Name	Stryker Trauma SA
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	false
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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Length	150 Millimeter
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Device Identifiers

Device Issuing Agency	Device ID
GS1	07613153051770 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K024060

FDA Product Code

HWC	Screw, fixation, bone