MANTIS 48486120

GUDID 04546540671585

HEX RAD ROD

Stryker Corporation

Bone-screw internal spinal fixation system, non-sterile

Primary Device ID	04546540671585
NIH Device Record Key	7b87ff89-0270-4a9e-845a-934b85025f9e
Commercial Distribution Status	In Commercial Distribution
Brand Name	MANTIS
Version Model Number	48486120
Catalog Number	48486120
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

Device Size Text, specify	0
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0
Length	120 Millimeter
Device Size Text, specify	0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540671585 [Primary]

FDA Product Code

NKB	Orthosis, spinal pedicle fixation, for degenerative disc disease