THOR 48035225

GUDID 07613327067460

COMPRESSION SCREW

Stryker Corporation

Spinal fixation plate, non-bioabsorbable

Primary Device ID	07613327067460
NIH Device Record Key	dea9cc39-4625-450d-80ca-7cfc0f4a5f6b
Commercial Distribution Status	In Commercial Distribution
Brand Name	THOR
Version Model Number	48035225
Catalog Number	48035225
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	07613327067460 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K073437

FDA Product Code

KWQ	APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY