LITe Plate System 49175544

GUDID 07613327066593

REVISION SCREW

Stryker Corporation

Spinal fixation plate, non-bioabsorbable

Primary Device ID	07613327066593
NIH Device Record Key	18dadcaa-d58e-490d-bf10-f6a951574b65
Commercial Distribution Status	In Commercial Distribution
Brand Name	LITe Plate System
Version Model Number	49175544
Catalog Number	49175544
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	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0
Length	44 Millimeter
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327066593 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K142699

FDA Product Code

KWQ	APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY