ENDOSKELETON® TT nanoLOCK® Surface Technology 4110-3507-N

GUDID 00191375012443

Interbody Fusion Device Parallel X-Large 7mm

TITAN SPINE, LLC

Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage
Primary Device ID00191375012443
NIH Device Record Key25d6e369-bbdf-437a-bc6d-ee7f641db450
Commercial Distribution StatusIn Commercial Distribution
Brand NameENDOSKELETON® TT nanoLOCK® Surface Technology
Version Model Number4110-3507-N
Catalog Number4110-3507-N
Company DUNS623316978
Company NameTITAN SPINE, LLC
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com
Phone+1(262)242-7801
Emailproductinfo@titanspine.com

Device Dimensions

Height7 Millimeter
Height7 Millimeter
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter
Depth11 Millimeter
Width35 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Height7 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100191375012443 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral fusion device with bone graft, lumbar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2020-02-24
Device Publish Date2016-12-15

On-Brand Devices [ENDOSKELETON® TT nanoLOCK® Surface Technology]

00191375012726Interbody Fusion Device 4 Degree X-Large 14mm
00191375012719Interbody Fusion Device 4 Degree X-Large 13mm
00191375012702Interbody Fusion Device 4 Degree X-Large 12mm
00191375012696Interbody Fusion Device 4 Degree X-Large 11mm
00191375012689Interbody Fusion Device 4 Degree X-Large 10mm
00191375012672Interbody Fusion Device 4 Degree X-Large 9mm
00191375012665Interbody Fusion Device 4 Degree X-Large 8mm
00191375012658Interbody Fusion Device 4 Degree Large 14mm
00191375012641Interbody Fusion Device 4 Degree Large 13mm
00191375012634Interbody Fusion Device 4 Degree Large 12mm
00191375012627Interbody Fusion Device 4 Degree Large 11mm
00191375012610Interbody Fusion Device 4 Degree Large 10mm
00191375012603Interbody Fusion Device 4 Degree Large 9mm
00191375012597Interbody Fusion Device 4 Degree Large 8mm
00191375012580Interbody Fusion Device 4 Degree Standard 14mm
00191375012573Interbody Fusion Device 4 Degree Standard 13mm
00191375012566Interbody Fusion Device 4 Degree Standard 12mm
00191375012559Interbody Fusion Device 4 Degree Standard 11mm
00191375012542Interbody Fusion Device 4 Degree Standard 10mm
00191375012535Interbody Fusion Device 4 Degree Standard 9mm
00191375012528Interbody Fusion Device 4 Degree Standard 8mm
00191375012511Interbody Fusion Device Parallel X-Large 14mm
00191375012504Interbody Fusion Device Parallel X-Large 13mm
00191375012498Interbody Fusion Device Parallel X-Large 12mm
00191375012481Interbody Fusion Device Parallel X-Large 11mm
00191375012474Interbody Fusion Device Parallel X-Large 10mm
00191375012467Interbody Fusion Device Parallel X-Large 9mm
00191375012450Interbody Fusion Device Parallel X-Large 8mm
00191375012443Interbody Fusion Device Parallel X-Large 7mm
00191375012436Interbody Fusion Device Parallel Large 14mm
00191375012429Interbody Fusion Device Parallel Large 13mm
00191375012412Interbody Fusion Device Parallel Large 12mm
00191375012405Interbody Fusion Device Parallel Large 11mm
00191375012399Interbody Fusion Device Parallel Large 10mm
00191375012382Interbody Fusion Device Parallel Large 9mm
00191375012375Interbody Fusion Device Parallel Large 8mm
00191375012368Interbody Fusion Device Parallel Large 7mm
00191375012351Interbody Fusion Device Parallel Standard 14mm
00191375012344Interbody Fusion Device Parallel Standard 13mm
00191375012337Interbody Fusion Device Parallel Standard 12mm
00191375012320Interbody Fusion Device Parallel Standard 11mm
00191375012313Interbody Fusion Device Parallel Standard 10mm
00191375012306Interbody Fusion Device Parallel Standard 9mm
00191375012290Interbody Fusion Device Parallel Standard 8mm
00191375012283Interbody Fusion Device Parallel Standard 7mm
00191375027317Interbody Fusion Device 4 Degree X-Large 7mm
00191375027300Interbody Fusion Device 4 Degree Large 7mm
00191375027294Interbody Fusion Device 4 Degree Standard 7mm

Trademark Results [ENDOSKELETON]

Mark Image

Registration | Serial
Company
Trademark
Application Date
ENDOSKELETON
ENDOSKELETON
76550301 3174488 Live/Registered
TITAN SPINE, INC.
2003-09-22
ENDOSKELETON
ENDOSKELETON
74130100 not registered Dead/Abandoned
CAROLCO PICTURES INC.
1991-01-14
ENDOSKELETON
ENDOSKELETON
74130099 1719530 Live/Registered
STUDIOCANAL, S.A.
1991-01-14
ENDOSKELETON
ENDOSKELETON
74124953 not registered Dead/Abandoned
CAROLCO PICTURES INC.
1990-12-20
ENDOSKELETON
ENDOSKELETON
74124952 not registered Dead/Abandoned
CAROLCO PICTURES INC.
1990-12-20

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