Primary Device ID | 00613994625328 |
NIH Device Record Key | 862cb180-6bf7-4a5d-a98a-e9fd5be2503e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ATLANTIS® Anterior Cervical Plate System |
Version Model Number | 7200050 |
Company DUNS | 830350380 |
Company Name | MEDTRONIC SOFAMOR DANEK, INC. |
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 | false |
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 |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Width | 50 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00613994625328 [Primary] |
KWQ | APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
[00613994625328]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-01 |
00613994866509 | PLATE 9010000224 ATL VIS ELITE 4LEV 75MM |
00613994866493 | PLATE 9010000223 ATL VIS ELT 3LEV 72.5MM |
00613994866486 | PLATE 9010000222 ATL VIS ELITE 3LEV 70MM |
00613994866479 | PLATE 9010000221 ATL VIS ELT 3LEV 67.5MM |
00613994866462 | PLATE 9010000220 ATL VIS ELITE 3LEV 65MM |
00613994866455 | PLATE 9010000219 ATL VIS ELT 3LEV 62.5MM |
00613994866448 | PLATE 9010000218 ATL VIS ELITE 3LEV 60MM |
00613994866431 | PLATE 9010000217 ATL VIS ELT 3LEV 57.5MM |
00613994866424 | PLATE 9010000216 ATL VIS ELITE 3LEV 55MM |
00613994866417 | PLATE 9010000215 ATL VIS ELT 3LEV 52.5MM |
00613994866400 | PLATE 9010000214 ATL VIS ELITE 2LEV 50MM |
00613994866394 | PLATE 9010000213 ATL VIS ELT 2LEV 47.5MM |
00613994866387 | PLATE 9010000212 ATL VIS ELITE 2LEV 45MM |
00613994866370 | PLATE 9010000211 ATL VIS ELT 2LEV 42.5MM |
00613994866363 | PLATE 9010000210 ATL VIS ELITE 2LEV 40MM |
00613994866356 | PLATE 9010000209 ATL VIS ELT 2LEV 37.5MM |
00613994866349 | PLATE 9010000208 ATL VIS ELITE 2LEV 35MM |
00613994866332 | PLATE 9010000207 ATL VIS ELT 2LEV 32.5MM |
00613994866325 | PLATE 9010000206 ATL VIS ELITE 1LEV 30MM |
00613994866318 | PLATE 9010000205 ATL VIS ELT 1LEV 27.5MM |
00613994866301 | PLATE 9010000204 ATL VIS ELITE 1LEV 25MM |
00613994866295 | PLATE 9010000203 ATL VIS ELITE 1LEV 23MM |
00613994866288 | PLATE 9010000202 ATL VIS ELITE 1LEV 21MM |
00613994866271 | PLATE 9010000201 ATL VIS ELITE 1LEV 19MM |
00613994866264 | PLATE 9010000234 ATL VIS ELITE 2LEV 40MM |
00613994866257 | PLATE 9010000233 ATL VIS ELT 2LEV 37.5MM |
00613994866240 | PLATE 9010000232 ATL VIS ELITE 2LEV 35MM |
00613994866233 | PLATE 9010000231 ATL VIS ELT 2LEV 32.5MM |
00613994866226 | PLATE 9010000230 ATL VIS ELITE 1LEV 30MM |
00613994866219 | PLATE 9010000229 ATL VIS ELT 1LEV 27.5MM |
00613994866202 | PLATE 9010000228 ATL VIS ELITE 1LEV 25MM |
00613994866196 | PLATE 9010000227 ATL VIS ELITE 1LEV 23MM |
00613994866189 | PLATE 9010000226 ATL VIS ELITE 1LEV 21MM |
00613994866172 | PLATE 9010000225 ATL VIS ELT 4LEV 77.5MM |
00613994857460 | CADDY X0810599 ST SCREW CADDY RD ELITE |
00613994857446 | CADDY X0810597 SD SCREW CADDY ELITE |
00613994625335 | PLATE 7200047 ATL VISION ELITE 47.5MM |
00613994625328 | PLATE 7200050 ATL VISION ELITE 50MM |
00613994625311 | PLATE 7200052 ATL VISION ELITE 52.5MM |
00613994625304 | PLATE 7200055 ATL VISION ELITE 55MM |
00613994625298 | PLATE 7200057 ATL VISION ELITE 57.5MM |
00613994625281 | PLATE 7200060 ATL VISION ELITE 60MM |
00613994625274 | PLATE 7200062 ATL VISION ELITE 62.5MM |
00613994625267 | PLATE 7200065 ATL VISION ELITE 65MM |
00613994625250 | PLATE 7200067 ATL VISION ELITE 67.5MM |
00613994625243 | PLATE 7200070 ATL VISION ELITE 70MM |
00613994625236 | PLATE 7200072 ATL VISION ELITE 72.5MM |
00613994625229 | PLATE 7200075 ATL VISION ELITE 75MM |
00613994625212 | PLATE 7200019 ATL VISION ELITE 19MM |
00613994625205 | PLATE 7200021 ATL VISION ELITE 21MM |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ATLANTIS 98395224 not registered Live/Pending |
ABELARES GROUP, LLC 2024-02-07 |
ATLANTIS 98395221 not registered Live/Pending |
ABELARES GROUP, LLC 2024-02-07 |
ATLANTIS 97800362 not registered Live/Pending |
Fowler, Timothy L. 2023-02-17 |
ATLANTIS 97681351 not registered Live/Pending |
BrainMaster Technologies, Inc. 2022-11-17 |
ATLANTIS 97636579 not registered Live/Pending |
Wenzhou Xiduoli Sanitary Ware Co., Ltd. 2022-10-18 |
ATLANTIS 97502702 not registered Live/Pending |
Kerzner International Resorts, Inc. 2022-07-14 |
ATLANTIS 97459185 not registered Live/Pending |
Atlantis Memorials B.V. 2022-06-15 |
ATLANTIS 90864327 not registered Live/Pending |
Kerzner International Resorts, Inc. 2021-08-04 |
ATLANTIS 90494735 not registered Live/Pending |
E V International ltd 2021-01-28 |
ATLANTIS 90232602 not registered Live/Pending |
CENTRE DE CONDITIONNEMENT PHYSIQUE ATLANTIS INC. 2020-10-02 |
ATLANTIS 90040152 not registered Live/Pending |
MS Directional, LLC 2020-07-07 |
ATLANTIS 88570065 not registered Live/Pending |
Vintae Luxury Wine Specialists, S.L.U. 2019-08-07 |