390021

GUDID 04546540066350

Cerclage Wire

Stryker Trauma SA

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Primary Device ID	04546540066350
NIH Device Record Key	5ec3c9e1-795e-47aa-aba2-e2ad1d680325
Commercial Distribution Status	In Commercial Distribution
Version Model Number	390021
Catalog Number	390021
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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540066350 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K914374

FDA Product Code

JDQ	CERCLAGE, FIXATION