ATLANTIS® Anterior Cervical Plate System

GUDID 00673978070612

SCREW 876-312 VAS CANCELLOUS 4.0X12MM

MEDTRONIC SOFAMOR DANEK, INC.

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00673978070612
NIH Device Record Keyfe6bf2b6-3bb8-4f98-9683-edf526c1c095
Commercial Distribution StatusIn Commercial Distribution
Brand NameATLANTIS® Anterior Cervical Plate System
Version Model Number876-312
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
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

Length12 Millimeter
Length12 Millimeter
Length12 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter
Outer Diameter4 Millimeter
Length12 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100673978070612 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

[00673978070612]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-08-19

On-Brand Devices [ATLANTIS® Anterior Cervical Plate System]

00613994866509PLATE 9010000224 ATL VIS ELITE 4LEV 75MM
00613994866493PLATE 9010000223 ATL VIS ELT 3LEV 72.5MM
00613994866486PLATE 9010000222 ATL VIS ELITE 3LEV 70MM
00613994866479PLATE 9010000221 ATL VIS ELT 3LEV 67.5MM
00613994866462PLATE 9010000220 ATL VIS ELITE 3LEV 65MM
00613994866455PLATE 9010000219 ATL VIS ELT 3LEV 62.5MM
00613994866448PLATE 9010000218 ATL VIS ELITE 3LEV 60MM
00613994866431PLATE 9010000217 ATL VIS ELT 3LEV 57.5MM
00613994866424PLATE 9010000216 ATL VIS ELITE 3LEV 55MM
00613994866417PLATE 9010000215 ATL VIS ELT 3LEV 52.5MM
00613994866400PLATE 9010000214 ATL VIS ELITE 2LEV 50MM
00613994866394PLATE 9010000213 ATL VIS ELT 2LEV 47.5MM
00613994866387PLATE 9010000212 ATL VIS ELITE 2LEV 45MM
00613994866370PLATE 9010000211 ATL VIS ELT 2LEV 42.5MM
00613994866363PLATE 9010000210 ATL VIS ELITE 2LEV 40MM
00613994866356PLATE 9010000209 ATL VIS ELT 2LEV 37.5MM
00613994866349PLATE 9010000208 ATL VIS ELITE 2LEV 35MM
00613994866332PLATE 9010000207 ATL VIS ELT 2LEV 32.5MM
00613994866325PLATE 9010000206 ATL VIS ELITE 1LEV 30MM
00613994866318PLATE 9010000205 ATL VIS ELT 1LEV 27.5MM
00613994866301PLATE 9010000204 ATL VIS ELITE 1LEV 25MM
00613994866295PLATE 9010000203 ATL VIS ELITE 1LEV 23MM
00613994866288PLATE 9010000202 ATL VIS ELITE 1LEV 21MM
00613994866271PLATE 9010000201 ATL VIS ELITE 1LEV 19MM
00613994866264PLATE 9010000234 ATL VIS ELITE 2LEV 40MM
00613994866257PLATE 9010000233 ATL VIS ELT 2LEV 37.5MM
00613994866240PLATE 9010000232 ATL VIS ELITE 2LEV 35MM
00613994866233PLATE 9010000231 ATL VIS ELT 2LEV 32.5MM
00613994866226PLATE 9010000230 ATL VIS ELITE 1LEV 30MM
00613994866219PLATE 9010000229 ATL VIS ELT 1LEV 27.5MM
00613994866202PLATE 9010000228 ATL VIS ELITE 1LEV 25MM
00613994866196PLATE 9010000227 ATL VIS ELITE 1LEV 23MM
00613994866189PLATE 9010000226 ATL VIS ELITE 1LEV 21MM
00613994866172PLATE 9010000225 ATL VIS ELT 4LEV 77.5MM
00613994857460CADDY X0810599 ST SCREW CADDY RD ELITE
00613994857446CADDY X0810597 SD SCREW CADDY ELITE
00613994625335PLATE 7200047 ATL VISION ELITE 47.5MM
00613994625328PLATE 7200050 ATL VISION ELITE 50MM
00613994625311PLATE 7200052 ATL VISION ELITE 52.5MM
00613994625304PLATE 7200055 ATL VISION ELITE 55MM
00613994625298PLATE 7200057 ATL VISION ELITE 57.5MM
00613994625281PLATE 7200060 ATL VISION ELITE 60MM
00613994625274PLATE 7200062 ATL VISION ELITE 62.5MM
00613994625267PLATE 7200065 ATL VISION ELITE 65MM
00613994625250PLATE 7200067 ATL VISION ELITE 67.5MM
00613994625243PLATE 7200070 ATL VISION ELITE 70MM
00613994625236PLATE 7200072 ATL VISION ELITE 72.5MM
00613994625229PLATE 7200075 ATL VISION ELITE 75MM
00613994625212PLATE 7200019 ATL VISION ELITE 19MM
00613994625205PLATE 7200021 ATL VISION ELITE 21MM

Trademark Results [ATLANTIS]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ATLANTIS
ATLANTIS
98395224 not registered Live/Pending
ABELARES GROUP, LLC
2024-02-07
ATLANTIS
ATLANTIS
98395221 not registered Live/Pending
ABELARES GROUP, LLC
2024-02-07
ATLANTIS
ATLANTIS
97800362 not registered Live/Pending
Fowler, Timothy L.
2023-02-17
ATLANTIS
ATLANTIS
97681351 not registered Live/Pending
BrainMaster Technologies, Inc.
2022-11-17
ATLANTIS
ATLANTIS
97636579 not registered Live/Pending
Wenzhou Xiduoli Sanitary Ware Co., Ltd.
2022-10-18
ATLANTIS
ATLANTIS
97502702 not registered Live/Pending
Kerzner International Resorts, Inc.
2022-07-14
ATLANTIS
ATLANTIS
97459185 not registered Live/Pending
Atlantis Memorials B.V.
2022-06-15
ATLANTIS
ATLANTIS
90864327 not registered Live/Pending
Kerzner International Resorts, Inc.
2021-08-04
ATLANTIS
ATLANTIS
90494735 not registered Live/Pending
E V International ltd
2021-01-28
ATLANTIS
ATLANTIS
90232602 not registered Live/Pending
CENTRE DE CONDITIONNEMENT PHYSIQUE ATLANTIS INC.
2020-10-02
ATLANTIS
ATLANTIS
90040152 not registered Live/Pending
MS Directional, LLC
2020-07-07
ATLANTIS
ATLANTIS
88570065 not registered Live/Pending
Vintae Luxury Wine Specialists, S.L.U.
2019-08-07
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