ENDOSKELETON® TA VBR nanoLOCK® Surface Technology 2107-0220-N

GUDID 00191375012016

Interbody Fusion Device 7 Degree Large 20mm

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 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 Metallic spinal interbody fusion cage
Primary Device ID00191375012016
NIH Device Record Key6789d139-6de6-49f8-9295-f16221a63c32
Commercial Distribution StatusIn Commercial Distribution
Brand NameENDOSKELETON® TA VBR nanoLOCK® Surface Technology
Version Model Number2107-0220-N
Catalog Number2107-0220-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
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0
Angle7 degree
Depth24 Millimeter
Width36 Millimeter
Device Size Text, specify0
Height20 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100191375012016 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQPSPINAL VERTEBRAL BODY REPLACEMENT DEVICE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2020-02-24
Device Publish Date2016-12-15

On-Brand Devices [ENDOSKELETON® TA VBR nanoLOCK® Surface Technology]

00191375012030Interbody Fusion Device 7 Degree X-Large 20mm
00191375012023Interbody Fusion Device 7 Degree X-Large 18mm
00191375012016Interbody Fusion Device 7 Degree Large 20mm
00191375012009Interbody Fusion Device 7 Degree Large 18mm
00191375011996Interbody Fusion Device 7 Degree Standard 20mm
00191375011989Interbody Fusion Device 7 Degree Standard 18mm

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
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.