XANTUS® Anterior Lateral Supplemental Fixation System
GUDID 00721902219535
PLATE 8967244 COVER PLATE 44MM
MEDTRONIC SOFAMOR DANEK, INC.
Bone-screw internal spinal fixation system, non-sterile| Primary Device ID | 00721902219535 |
| NIH Device Record Key | 8a11ac8f-4f3c-49a4-a7db-36d17a2a6043 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | XANTUS® Anterior Lateral Supplemental Fixation System |
| Version Model Number | 8967244 |
| 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 |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00721902219535 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K014267
FDA Product Code
| KWP | APPLIANCE, FIXATION, SPINAL INTERLAMINAL |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
[00721902219535]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-07-30 |
On-Brand Devices [XANTUS® Anterior Lateral Supplemental Fixation System]
| 00721902227394 | FIXE ANGLE LOCKING PLATE 60MM |
| 00721902226786 | FIXE ANGLE LOCKING PLATE 56MM |
| 00721902225796 | FIXE ANGLE LOCKING PLATE 52MM |
| 00721902225345 | FIXE ANGLE LOCKING PLATE 48MM |
| 00721902225000 | FIXE ANGLE LOCKING PLATE 44MM |
| 00721902224058 | PLATE 8967260 COVER PLATE 60MM |
| 00721902222962 | PLATE 8967256 COVER PLATE 56MM |
| 00721902222283 | PLATE 8967252 COVER PLATE 52MM |
| 00721902221927 | PLATE 8967248 COVER PLATE 48MM |
| 00721902219535 | PLATE 8967244 COVER PLATE 44MM |
| 00721902216077 | PLATE 8967160 PLATE 60MM |
| 00721902215704 | PLATE 8967156 PLATE 56MM |
| 00721902215261 | PLATE 8967152 PLATE 52MM |
| 00721902214707 | PLATE 8967148 PLATE 48MM |
| 00721902214691 | PLATE 8967144 PLATE 44MM |
Trademark Results [XANTUS]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 XANTUS 98242076 not registered Live/Pending |
Kim Einsenmann 2023-10-26 |
XANTUS 98242076 not registered Live/Pending |
Sven Haeusler 2023-10-26 |
 XANTUS 85365706 4185262 Dead/Cancelled |
BAYSPEC, INC. 2011-07-07 |
 XANTUS 85072189 not registered Dead/Abandoned |
Insitu, Inc. 2010-06-25 |
 XANTUS 79280465 not registered Live/Pending |
Twinvay GmbH 2020-01-16 |
 XANTUS 79183126 5148512 Live/Registered |
Tecan Schweiz AG 2015-12-03 |
 XANTUS 78107312 2846433 Dead/Cancelled |
MEDTRONIC SOFAMOR DANEK, INC. 2002-02-07 |
 XANTUS 75487237 2358388 Dead/Cancelled |
Phoenix Healthcare Corporation 1998-05-18 |
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