ENDOSKELETON® TAS 2312-0211

GUDID 00191375001676

Interbody Fusion Device 12 Degree Large 11mm

TITAN SPINE, LLC

Metallic spinal fusion cage, non-sterile
Primary Device ID00191375001676
NIH Device Record Key625a6c8c-6a53-4bd9-8de2-03cc00b44844
Commercial Distribution StatusIn Commercial Distribution
Brand NameENDOSKELETON® TAS
Version Model Number2312-0211
Catalog Number2312-0211
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 Datefalse
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

Device Dimensions

Height11 Millimeter
Height11 Millimeter
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter
Device Size Text, specify0
Width36 Millimeter
Angle12 degree
Depth24 Millimeter
Device Size Text, specify0
Height11 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100191375001676 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OVDIntervertebral fusion device with integrated fixation, lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


[00191375001676]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-07-17
Device Publish Date2016-12-15

On-Brand Devices [ENDOSKELETON® TAS]

00191375028253Hyperlordotic Instrument Tray Sys, 16, 20°
00191375028246Hyperlordotic Instrument Tray System, 16, 20, 24°
00191375028239Hyperlordotic, One-Up, Anterolateral Inserter
00191375028222Hyperlordotic, Two-Up, Anterolateral Inserter
0019137502821524 Deg Lordotic, Rasp, X-Large, 20mm
0019137502820824 Deg Lordotic, Rasp, X-Large, 18mm
0019137502819224 Deg Lordotic, Rasp, X-Large, 16mm
0019137502818524 Deg Lordotic, Rasp, X-Large, 14mm
0019137502817824 Deg Lordotic, Rasp, Large, 20mm
0019137502816124 Deg Lordotic, Rasp, Large, 18mm
0019137502815424 Deg Lordotic, Rasp, Large, 16mm
0019137502814724 Deg Lordotic, Rasp, Large, 14mm
0019137502813024 Deg Lordotic, Rasp, Standard, 20mm
0019137502812324 Deg Lordotic, Rasp, Standard, 18mm
0019137502811624 Deg Lordotic, Rasp, Standard, 16mm
0019137502810924 Deg Lordotic, Rasp, Standard, 14mm
0019137502809320 Deg Lordotic, Rasp, X-Large, 20mm
0019137502808620 Deg Lordotic, Rasp, X-Large, 18mm
0019137502807920 Deg Lordotic, Rasp, X-Large, 16mm
0019137502806220 Deg Lordotic, Rasp, X-Large, 14mm
0019137502805520 Deg Lordotic, Rasp, X-Large, 12mm
0019137502804820 Deg Lordotic, Rasp, Large, 20mm
0019137502803120 Deg Lordotic, Rasp, Large, 18mm
0019137502802420 Deg Lordotic, Rasp, Large, 16mm
0019137502801720 Deg Lordotic, Rasp, Large, 14mm
0019137502800020 Deg Lordotic, Rasp, Large, 12mm
0019137502799720 Deg Lordotic, Rasp, Standard, 20mm
0019137502798020 Deg Lordotic, Rasp, Standard, 18mm
0019137502797320 Deg Lordotic, Rasp, Standard, 16mm
0019137502796620 Deg Lordotic, Rasp, Standard, 14mm
0019137502795920 Deg Lordotic, Rasp, Standard, 12mm
0019137502794216 Deg Lordotic, Rasp, X-Large, 20mm
0019137502793516 Deg Lordotic, Rasp, X-Large, 18mm
0019137502792816 Deg Lordotic, Rasp, X-Large, 16mm
0019137502791116 Deg Lordotic, Rasp, X-Large, 14mm
0019137502790416 Deg Lordotic, Rasp, X-Large, 12mm
0019137502789816 Deg Lordotic, Rasp, X-Large, 10mm
0019137502788116 Deg Lordotic, Rasp, Large, 20mm
0019137502787416 Deg Lordotic, Rasp, Large, 18mm
0019137502786716 Deg Lordotic, Rasp, Large, 16mm
0019137502785016 Deg Lordotic, Rasp, Large, 14mm
0019137502784316 Deg Lordotic, Rasp, Large, 12mm
0019137502783616 Deg Lordotic, Rasp, Large, 10mm
0019137502782916 Deg Lordotic, Rasp, Standard, 20mm
0019137502781216 Deg Lordotic, Rasp, Standard, 18mm
0019137502780516 Deg Lordotic, Rasp, Standard, 16mm
0019137502779916 Deg Lordotic, Rasp, Standard, 14mm
0019137502778216 Deg Lordotic, Rasp, Standard, 12mm
0019137502777516 Deg Lordotic, Rasp, Standard, 10mm
00191375027737Interbody Fusion Device 6.5mm Implant Bone Screw 35mm

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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