ENDOSKELETON® TA nanoLOCK® Surface Technology 2107-0110-N
GUDID 00191375012047
Interbody Fusion Device 7 Degree Standard 10mm
TITAN SPINE, LLC
Metallic spinal interbody fusion cage| Primary Device ID | 00191375012047 |
| NIH Device Record Key | 9618a4c2-d661-41bb-837e-c700e08630de |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ENDOSKELETON® TA nanoLOCK® Surface Technology |
| Version Model Number | 2107-0110-N |
| Catalog Number | 2107-0110-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
| Height | 10 Millimeter |
| Height | 10 Millimeter |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
| Width | 32 Millimeter |
| Depth | 21 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Device Size Text, specify | 0 |
| Height | 10 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00191375012047 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K080615
FDA Product Code
| MAX | Intervertebral fusion device with bone graft, 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 | 6 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2016-12-15 |
On-Brand Devices [ENDOSKELETON® TA nanoLOCK® Surface Technology]
| 00191375012276 | Interbody Fusion Device 7 Degree X-Large 17mm |
| 00191375012269 | Interbody Fusion Device 7 Degree X-Large 16mm |
| 00191375012252 | Interbody Fusion Device 7 Degree X-Large 15mm |
| 00191375012245 | Interbody Fusion Device 7 Degree X-Large 14mm |
| 00191375012238 | Interbody Fusion Device 7 Degree X-Large 13mm |
| 00191375012221 | Interbody Fusion Device 7 Degree X-Large 12mm |
| 00191375012214 | Interbody Fusion Device 7 Degree X-Large 11mm |
| 00191375012207 | Interbody Fusion Device 7 Degree X-Large 10mm |
| 00191375012191 | Interbody Fusion Device 7 Degree Large 17mm |
| 00191375012184 | Interbody Fusion Device 7 Degree Large 16mm |
| 00191375012177 | Interbody Fusion Device 7 Degree Large 15mm |
| 00191375012160 | Interbody Fusion Device 7 Degree Large 14mm |
| 00191375012153 | Interbody Fusion Device 7 Degree Large 13mm |
| 00191375012146 | Interbody Fusion Device 7 Degree Large 12mm |
| 00191375012139 | Interbody Fusion Device 7 Degree Large 11mm |
| 00191375012122 | Interbody Fusion Device 7 Degree Large 10mm |
| 00191375012115 | Interbody Fusion Device 7 Degree Standard 17mm |
| 00191375012108 | Interbody Fusion Device 7 Degree Standard 16mm |
| 00191375012092 | Interbody Fusion Device 7 Degree Standard 15mm |
| 00191375012085 | Interbody Fusion Device 7 Degree Standard 14mm |
| 00191375012078 | Interbody Fusion Device 7 Degree Standard 13mm |
| 00191375012061 | Interbody Fusion Device 7 Degree Standard 12mm |
| 00191375012054 | Interbody Fusion Device 7 Degree Standard 11mm |
| 00191375012047 | Interbody Fusion Device 7 Degree Standard 10mm |
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 |
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