ATLANTIS ® Anterior Cervical Plate System
GUDID 00673978010601
CASE 176-502 ATLANTIS CASE LID
MEDTRONIC SOFAMOR DANEK, INC.
Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable| Primary Device ID | 00673978010601 |
| NIH Device Record Key | 4e666980-4d28-458b-9ce9-59b266a311b2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ATLANTIS ® Anterior Cervical Plate System |
| Version Model Number | 176-502 |
| Company DUNS | 830350380 |
| Company Name | MEDTRONIC SOFAMOR DANEK, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| 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 | false |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00673978010601 [Primary] |
FDA Product Code
| FSM | TRAY, SURGICAL, INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
[00673978010601]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-08-09 |
| Device Publish Date | 2017-10-06 |
On-Brand Devices [ATLANTIS ® Anterior Cervical Plate System]
| 00613994466358 | SCREW X1107035 4.25 X 15 SD VAS |
| 00613994466341 | SCREW X1107034 4.25 X 14 SD VAS |
| 00613994466334 | SCREW X1107033 4.25 X 13 SD VAS |
| 00613994466327 | SCREW X1107032 4.25 X 12 SD VAS |
| 00613994383822 | PLATE X0607174 ATL - 30MM - 1 LEV |
| 00613994383808 | PLATE X0607176 ATL - 35MM - 1 LEV |
| 00613994383785 | PLATE X0607178 ATL - 40MM - 1 LEV |
| 00613994383747 | PLATE X0607182 ATL - 87.5MM - 4 LEV |
| 00613994383730 | PLATE X0607183 ATL - 90MM - 4 LEV |
| 00613994383723 | PLATE X0607184 ATL - 92.5MM - 4 LEV |
| 00613994383716 | PLATE X0607185 ATL - 95MM - 4 LEV |
| 00673978010687 | CASE 176-510 ATLANTIS UPPER INS TRAY |
| 00673978010670 | CASE 176-509 ATLANTIS PLATE TRAY LID |
| 00673978010601 | CASE 176-502 ATLANTIS CASE LID |
Trademark Results [ATLANTIS]
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 |
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.