ATLANTIS(TM) VISION Anterior Cervical Plate

GUDID 00721902725173

ATL VIS PLT-12/2-110MM-5LEV

MEDTRONIC SOFAMOR DANEK, INC.

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00721902725173
NIH Device Record Key61dba61e-bb71-4143-87bc-98798451ca45
Commercial Distribution StatusIn Commercial Distribution
Brand NameATLANTIS(TM) VISION Anterior Cervical Plate
Version Model NumberX1002110
Company DUNS830350380
Company NameMEDTRONIC SOFAMOR DANEK, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter
Width110 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100721902725173 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

[00721902725173]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-08-18

On-Brand Devices [ATLANTIS(TM) VISION Anterior Cervical Plate]

00721902725173ATL VIS PLT-12/2-110MM-5LEV
00721902725166ATL VIS PLT-12/2-105MM-5LEV
00721902725159ATL VIS PLT-12/2-100MM-5LEV
00721902725142ATL VIS PLT-12/2-95MM-5LEV
00721902725135ATL VIS PLT-12/2-90MM-5LEV
00721902725128ATL VIS PLT-12/2-87.5MM-5LEV
00721902725111ATL VIS PLT-12/2-85MM-4LEV
00721902725098ATL VIS PLT-12/2-82.5MM-4LEV
00721902725081ATL VIS PLT-12/2-80MM-4LEV
00721902725074ATL VIS PLT-12/2-77.5MM-4LEV
00721902725012ATL VIS PLT-12/2-75MM-4LEV
00721902725005ATL VIS PLT-12/2-72.5MM-3LEV
00721902724992ATL VIS PLT-12/2-70MM-3LEV
00721902724985ATL VIS PLT-12/2-67.5MM-3LEV
00721902724978ATL VIS PLT-12/2-65MM-3LEV
00721902724961ATL VIS PLT-12/2-62.5MM-3LEV
00721902724954ATL VIS PLT-12/2-60MM-3LEV
00721902724947ATL VIS PLT-12/2-57.5MM-3LEV
00721902724787ATL VIS PLT-12/2-55MM-3LEV
00721902724770ATL VIS PLT-12/2-52.5MM-3LEV
00721902724763ATL VIS PLT-12/2-50MM-2LEV
00721902724756ATL VIS PLT-12/2-47.5MM-2LEV
00721902724749ATL VIS PLT-12/2-45MM-2LEV
00721902724282ATL VIS PLT-12/2-42.5MM-2LEV
00721902724251ATL VIS PLT-12/2-40MM-2LEV
00721902724190ATL VIS PLT-12/2-37.5MM-2LEV
00721902724169ATL VIS PLT-12/2-35MM-2LEV
00721902724152ATL VIS PLT-12/2-32.5MM-2LEV
00721902724138ATL VIS PLT-12/2-30MM-1LEV
00721902724107ATL VIS PLT-12/2-27MM-1LEV
00721902724091ATL VIS PLT-12/2-25MM-1LEV
00721902724084ATL VIS PLT-12/2-23MM-1LEV
00721902724060ATL VIS PLT-12/2-21MM-1LEV
00721902724053ATL VIS PLT-12/2-19MM-1LEV
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