ENDOSKELETON® TAS nanoLOCK® Surface Technology 2307-0117-N
GUDID 00191375013822
Interbody Fusion Device 7 Degree Standard 17mm
TITAN SPINE, LLC
Metallic spinal interbody fusion cage| Primary Device ID | 00191375013822 |
| NIH Device Record Key | 83034ffd-69b5-4528-87d1-c79db34fc4de |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ENDOSKELETON® TAS nanoLOCK® Surface Technology |
| Version Model Number | 2307-0117-N |
| Catalog Number | 2307-0117-N |
| Company DUNS | 623316978 |
| Company Name | TITAN SPINE, LLC |
| Device Count | 1 |
| DM Exempt | true |
| 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 | true |
| Expiration Date | true |
| 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 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Depth | 21 Millimeter |
| Width | 32 Millimeter |
| Height | 17 Millimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00191375013822 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
FDA Product Code
| OVD | Intervertebral fusion device with integrated fixation, lumbar |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2016-12-15 |
On-Brand Devices [ENDOSKELETON® TAS nanoLOCK® Surface Technology]
| 00191375014300 | Interbody Fusion Device 12 Degree X-Large 17mm |
| 00191375014294 | Interbody Fusion Device 12 Degree X-Large 16mm |
| 00191375014287 | Interbody Fusion Device 12 Degree X-Large 15mm |
| 00191375014270 | Interbody Fusion Device 12 Degree X-Large 14mm |
| 00191375014263 | Interbody Fusion Device 12 Degree X-Large 13mm |
| 00191375014256 | Interbody Fusion Device 12 Degree X-Large 12mm |
| 00191375014249 | Interbody Fusion Device 12 Degree X-Large 11mm |
| 00191375014232 | Interbody Fusion Device 12 Degree X-Large 10mm |
| 00191375014225 | Interbody Fusion Device 12 Degree Large 17mm |
| 00191375014218 | Interbody Fusion Device 12 Degree Large 16mm |
| 00191375014201 | Interbody Fusion Device 12 Degree Large 15mm |
| 00191375014195 | Interbody Fusion Device 12 Degree Large 14mm |
| 00191375014188 | Interbody Fusion Device 12 Degree Large 13mm |
| 00191375014171 | Interbody Fusion Device 12 Degree Large 12mm |
| 00191375014164 | Interbody Fusion Device 12 Degree Large 11mm |
| 00191375014157 | Interbody Fusion Device 12 Degree Large 10mm |
| 00191375014140 | Interbody Fusion Device 12 Degree Standard 17mm |
| 00191375014133 | Interbody Fusion Device 12 Degree Standard 16mm |
| 00191375014126 | Interbody Fusion Device 12 Degree Standard 15mm |
| 00191375014119 | Interbody Fusion Device 12 Degree Standard 14mm |
| 00191375014102 | Interbody Fusion Device 12 Degree Standard 13mm |
| 00191375014096 | Interbody Fusion Device 12 Degree Standard 12mm |
| 00191375014089 | Interbody Fusion Device 12 Degree Standard 11mm |
| 00191375014072 | Interbody Fusion Device 12 Degree Standard 10mm |
| 00191375014065 | Interbody Fusion Device 12 Degree Hybrid 17mm |
| 00191375014058 | Interbody Fusion Device 12 Degree Hybrid 16mm |
| 00191375014041 | Interbody Fusion Device 12 Degree Hybrid 15mm |
| 00191375014034 | Interbody Fusion Device 12 Degree Hybrid 14mm |
| 00191375014027 | Interbody Fusion Device 12 Degree Hybrid 13mm |
| 00191375014010 | Interbody Fusion Device 12 Degree Hybrid 12mm |
| 00191375014003 | Interbody Fusion Device 12 Degree Hybrid 11mm |
| 00191375013990 | Interbody Fusion Device 12 Degree Hybrid 10mm |
| 00191375013983 | Interbody Fusion Device 7 Degree X-Large 17mm |
| 00191375013976 | Interbody Fusion Device 7 Degree X-Large 16mm |
| 00191375013969 | Interbody Fusion Device 7 Degree X-Large 15mm |
| 00191375013952 | Interbody Fusion Device 7 Degree X-Large 14mm |
| 00191375013945 | Interbody Fusion Device 7 Degree X-Large 13mm |
| 00191375013938 | Interbody Fusion Device 7 Degree X-Large 12mm |
| 00191375013921 | Interbody Fusion Device 7 Degree X-Large 11mm |
| 00191375013914 | Interbody Fusion Device 7 Degree X-Large 10mm |
| 00191375013907 | Interbody Fusion Device 7 Degree Large 17mm |
| 00191375013891 | Interbody Fusion Device 7 Degree Large 16mm |
| 00191375013884 | Interbody Fusion Device 7 Degree Large 15mm |
| 00191375013877 | Interbody Fusion Device 7 Degree Large 14mm |
| 00191375013860 | Interbody Fusion Device 7 Degree Large 13mm |
| 00191375013853 | Interbody Fusion Device 7 Degree Large 12mm |
| 00191375013846 | Interbody Fusion Device 7 Degree Large 11mm |
| 00191375013839 | Interbody Fusion Device 7 Degree Large 10mm |
| 00191375013822 | Interbody Fusion Device 7 Degree Standard 17mm |
| 00191375013815 | Interbody Fusion Device 7 Degree Standard 16mm |
Trademark Results [ENDOSKELETON]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ENDOSKELETON 76550301 3174488 Live/Registered |
TITAN SPINE, INC. 2003-09-22 |
 ENDOSKELETON 74130100 not registered Dead/Abandoned |
CAROLCO PICTURES INC. 1991-01-14 |
 ENDOSKELETON 74130099 1719530 Live/Registered |
STUDIOCANAL, S.A. 1991-01-14 |
 ENDOSKELETON 74124953 not registered Dead/Abandoned |
CAROLCO PICTURES INC. 1990-12-20 |
 ENDOSKELETON 74124952 not registered Dead/Abandoned |
CAROLCO PICTURES INC. 1990-12-20 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.