ENDOSKELETON® TL nanoLOCK® Surface Technology 7107-2112-N
GUDID 00191375016762
Interbody Fusion Device 7 Degree 40 (M/L) 26 (A/P) 12 mm
TITAN SPINE, LLC
Metallic spinal interbody fusion cage| Primary Device ID | 00191375016762 |
| NIH Device Record Key | f374399a-5bdc-46de-afe1-3553bcbe2ab2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ENDOSKELETON® TL nanoLOCK® Surface Technology |
| Version Model Number | 7107-2112-N |
| Catalog Number | 7107-2112-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
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com | |
| Phone | +1(262)242-7801 |
| productinfo@titanspine.com |
Device Dimensions
| Height | 12 Millimeter |
| Height | 12 Millimeter |
| Height | 12 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
| Device Size Text, specify | 0 |
| Angle | 7 degree |
| Length | 40 Millimeter |
| Device Size Text, specify | 0 |
| Width | 26 Millimeter |
| Height | 12 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00191375016762 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K140055
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 | 5 |
| Public Version Date | 2020-02-24 |
| Device Publish Date | 2016-12-15 |
On-Brand Devices [ENDOSKELETON® TL nanoLOCK® Surface Technology]
| 00191375018353 | Interbody Fusion Device 12 Degree 60 (M/L) 26 (A/P) 16 mm |
| 00191375018346 | Interbody Fusion Device 12 Degree 55 (M/L) 26 (A/P) 16 mm |
| 00191375018339 | Interbody Fusion Device 12 Degree 50 (M/L) 26 (A/P) 16 mm |
| 00191375018322 | Interbody Fusion Device 12 Degree 45 (M/L) 26 (A/P) 16 mm |
| 00191375018315 | Interbody Fusion Device 12 Degree 40 (M/L) 26 (A/P) 16 mm |
| 00191375018308 | Interbody Fusion Device 12 Degree 60 (M/L) 26 (A/P) 15 mm |
| 00191375018292 | Interbody Fusion Device 12 Degree 55 (M/L) 26 (A/P) 15 mm |
| 00191375018285 | Interbody Fusion Device 12 Degree 50 (M/L) 26 (A/P) 15 mm |
| 00191375018278 | Interbody Fusion Device 12 Degree 45 (M/L) 26 (A/P) 15 mm |
| 00191375018261 | Interbody Fusion Device 12 Degree 40 (M/L) 26 (A/P) 15 mm |
| 00191375018254 | Interbody Fusion Device 12 Degree 60 (M/L) 26 (A/P) 14 mm |
| 00191375018247 | Interbody Fusion Device 12 Degree 55 (M/L) 26 (A/P) 14 mm |
| 00191375018230 | Interbody Fusion Device 12 Degree 50 (M/L) 26 (A/P) 14 mm |
| 00191375018223 | Interbody Fusion Device 12 Degree 45 (M/L) 26 (A/P) 14 mm |
| 00191375018216 | Interbody Fusion Device 12 Degree 40 (M/L) 26 (A/P) 14 mm |
| 00191375018209 | Interbody Fusion Device 12 Degree 60 (M/L) 26 (A/P) 13 mm |
| 00191375018193 | Interbody Fusion Device 12 Degree 55 (M/L) 26 (A/P) 13 mm |
| 00191375018186 | Interbody Fusion Device 12 Degree 50 (M/L) 26 (A/P) 13 mm |
| 00191375018179 | Interbody Fusion Device 12 Degree 45 (M/L) 26 (A/P) 13 mm |
| 00191375018162 | Interbody Fusion Device 12 Degree 40 (M/L) 26 (A/P) 13 mm |
| 00191375018155 | Interbody Fusion Device 12 Degree 60 (M/L) 26 (A/P) 12 mm |
| 00191375018148 | Interbody Fusion Device 12 Degree 55 (M/L) 26 (A/P) 12 mm |
| 00191375018131 | Interbody Fusion Device 12 Degree 50 (M/L) 26 (A/P) 12 mm |
| 00191375018124 | Interbody Fusion Device 12 Degree 45 (M/L) 26 (A/P) 12 mm |
| 00191375018117 | Interbody Fusion Device 12 Degree 40 (M/L) 26 (A/P) 12 mm |
| 00191375018100 | Interbody Fusion Device 12 Degree 60 (M/L) 26 (A/P) 11 mm |
| 00191375018094 | Interbody Fusion Device 12 Degree 55 (M/L) 26 (A/P) 11 mm |
| 00191375018087 | Interbody Fusion Device 12 Degree 50 (M/L) 26 (A/P) 11 mm |
| 00191375018070 | Interbody Fusion Device 12 Degree 45 (M/L) 26 (A/P) 11 mm |
| 00191375018063 | Interbody Fusion Device 12 Degree 40 (M/L) 26 (A/P) 11 mm |
| 00191375018056 | Interbody Fusion Device 12 Degree 60 (M/L) 26 (A/P) 10 mm |
| 00191375018049 | Interbody Fusion Device 12 Degree 55 (M/L) 26 (A/P) 10 mm |
| 00191375018032 | Interbody Fusion Device 12 Degree 50 (M/L) 26 (A/P) 10 mm |
| 00191375018025 | Interbody Fusion Device 12 Degree 45 (M/L) 26 (A/P) 10 mm |
| 00191375018018 | Interbody Fusion Device 12 Degree 40 (M/L) 26 (A/P) 10 mm |
| 00191375018001 | Interbody Fusion Device 12 Degree 60 (M/L) 26 (A/P) 9 mm |
| 00191375017998 | Interbody Fusion Device 12 Degree 55 (M/L) 26 (A/P) 9 mm |
| 00191375017981 | Interbody Fusion Device 12 Degree 50 (M/L) 26 (A/P) 9 mm |
| 00191375017974 | Interbody Fusion Device 12 Degree 45 (M/L) 26 (A/P) 9 mm |
| 00191375017967 | Interbody Fusion Device 12 Degree 40 (M/L) 26 (A/P) 9 mm |
| 00191375017950 | Interbody Fusion Device 12 Degree 60 (M/L) 26 (A/P) 8 mm |
| 00191375017943 | Interbody Fusion Device 12 Degree 55 (M/L) 26 (A/P) 8 mm |
| 00191375017936 | Interbody Fusion Device 12 Degree 50 (M/L) 26 (A/P) 8 mm |
| 00191375017929 | Interbody Fusion Device 12 Degree 45 (M/L) 26 (A/P) 8 mm |
| 00191375017912 | Interbody Fusion Device 12 Degree 40 (M/L) 26 (A/P) 8 mm |
| 00191375017905 | Interbody Fusion Device 12 Degree 60 (M/L) 22 (A/P) 16 mm |
| 00191375017899 | Interbody Fusion Device 12 Degree 55 (M/L) 22 (A/P) 16 mm |
| 00191375017882 | Interbody Fusion Device 12 Degree 50 (M/L) 22 (A/P) 16 mm |
| 00191375017875 | Interbody Fusion Device 12 Degree 45 (M/L) 22 (A/P) 16 mm |
| 00191375017868 | Interbody Fusion Device 12 Degree 40 (M/L) 22 (A/P) 16 mm |
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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