MANTIS 48288130

GUDID 07613154722013

STRAIGHT ROD

Stryker Corporation

Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod Bone-screw internal spinal fixation system rod

Primary Device ID	07613154722013
NIH Device Record Key	209d8e3c-bda6-448e-983f-d38acb069e81
Commercial Distribution Status	In Commercial Distribution
Brand Name	MANTIS
Version Model Number	48288130
Catalog Number	48288130
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	07613154722013 [Primary]

FDA Product Code

NKB	Orthosis, spinal pedicle fixation, for degenerative disc disease