MANTIS Redux 48289635

GUDID 04546540671172

POLYAXIAL REDUCTION SCREW

Stryker Corporation

Bone-screw internal spinal fixation system, non-sterile

Primary Device ID	04546540671172
NIH Device Record Key	d7d477f1-e324-46c6-80e0-38b6174ef4d0
Commercial Distribution Status	In Commercial Distribution
Brand Name	MANTIS Redux
Version Model Number	48289635
Catalog Number	48289635
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	04546540671172 [Primary]

FDA Product Code

KWP	APPLIANCE, FIXATION, SPINAL INTERLAMINAL