ENDOSKELETON® TT 4110-3007
GUDID 00191375002611
Interbody Fusion Device Parallel Large 7mm
TITAN SPINE, LLC
Metallic spinal fusion cage, non-sterile| Primary Device ID | 00191375002611 |
| NIH Device Record Key | 6b58ab77-c2b7-44e2-987a-7c6c2bf875bc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ENDOSKELETON® TT |
| Version Model Number | 4110-3007 |
| Catalog Number | 4110-3007 |
| 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 | 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 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
| Depth | 11 Millimeter |
| Device Size Text, specify | 0 |
| Width | 30 Millimeter |
| Height | 7 Millimeter |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00191375002611 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K083714
FDA Product Code
| MAX | Intervertebral fusion device with bone graft, lumbar |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
[00191375002611]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-07-17 |
| Device Publish Date | 2016-12-15 |
On-Brand Devices [ENDOSKELETON® TT]
| 00191375028277 | Expandable Distractor |
| 00191375028260 | Expandable Distractor Tray System |
| 00191375003304 | Implant Caddy |
| 00191375003298 | 7mm Caddy |
| 00191375003281 | TLIF Tray System |
| 00191375003274 | Surgical Tray System |
| 00191375003267 | Trial, Parallel, Curved, 7mm |
| 00191375003250 | Trial, Parallel, Curved, 6mm |
| 00191375003243 | Trial, 4 Deg Lordotic, Curved, 14mm |
| 00191375003236 | Trial, 4 Deg Lordotic, Curved, 13mm |
| 00191375003229 | Trial, 4 Deg Lordotic, Curved, 12mm |
| 00191375003212 | Trial, 4 Deg Lordotic, Curved, 11mm |
| 00191375003205 | Trial, 4 Deg Lordotic, Curved, 10mm |
| 00191375003199 | Trial, 4 Deg Lordotic, Curved, 9mm |
| 00191375003182 | Trial, 4 Deg Lordotic, Curved, 8mm |
| 00191375003168 | Shaver, 14mm |
| 00191375003151 | Shaver, 13mm |
| 00191375003144 | Shaver, 12mm |
| 00191375003137 | Shaver, 11mm |
| 00191375003120 | Shaver, 10mm |
| 00191375003113 | Shaver, 9mm |
| 00191375003106 | Shaver, 8mm |
| 00191375003090 | Shaver, 7mm |
| 00191375003083 | Hudson, Locking T-Handle |
| 00191375003076 | Ring Curette, 8mm |
| 00191375003069 | Large Angled Down Curette |
| 00191375003052 | Large Angled Left Curette |
| 00191375003045 | Large Angled Right Curette |
| 00191375003038 | Large Straight Curette |
| 00191375003021 | Osteotome |
| 00191375003014 | Thin Implant Pusher |
| 00191375003007 | Straight Pusher |
| 00191375002994 | Curved Implant Holder |
| 00191375002987 | Implant Holder Assembly, Straight |
| 00191375002970 | Interbody Fusion Device 4 Degree X-Large 14mm |
| 00191375002963 | Interbody Fusion Device 4 Degree X-Large 13mm |
| 00191375002956 | Interbody Fusion Device 4 Degree X-Large 12mm |
| 00191375002949 | Interbody Fusion Device 4 Degree X-Large 11mm |
| 00191375002932 | Interbody Fusion Device 4 Degree X-Large 10mm |
| 00191375002925 | Interbody Fusion Device 4 Degree X-Large 9mm |
| 00191375002918 | Interbody Fusion Device 4 Degree X-Large 8mm |
| 00191375002901 | Interbody Fusion Device 4 Degree Large 14mm |
| 00191375002895 | Interbody Fusion Device 4 Degree Large 13mm |
| 00191375002888 | Interbody Fusion Device 4 Degree Large 12mm |
| 00191375002871 | Interbody Fusion Device 4 Degree Large 11mm |
| 00191375002864 | Interbody Fusion Device 4 Degree Large 10mm |
| 00191375002857 | Interbody Fusion Device 4 Degree Large 9mm |
| 00191375002840 | Interbody Fusion Device 4 Degree Large 8mm |
| 00191375002833 | Interbody Fusion Device 4 Degree Standard 14mm |
| 00191375002826 | Interbody Fusion Device 4 Degree Standard 13mm |
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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