ES2 SPINAL SYSTEM 482805070

GUDID 07613327066906

VITALLIUM 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

Primary Device ID	07613327066906
NIH Device Record Key	67247846-6a18-461c-8385-a9a4f8b8db9c
Commercial Distribution Status	In Commercial Distribution
Brand Name	ES2 SPINAL SYSTEM
Version Model Number	482805070
Catalog Number	482805070
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	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0
Length	70 Millimeter
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327066906 [Primary]

FDA Product Code

NKB	Orthosis, spinal pedicle fixation, for degenerative disc disease