TrellOss™-L MPF

GUDID 00840067206645

Lateral 40Lx22Wx14H 30°

NEXXT 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
Primary Device ID00840067206645
NIH Device Record Key96b5251d-148b-493e-a76a-b7813368357f
Commercial Distribution StatusIn Commercial Distribution
Brand NameTrellOss™-L MPF
Version Model Number162H4014
Company DUNS003489810
Company NameNEXXT SPINE, LLC
Device Count1
DM Exemptfalse
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

Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com
Phone317-436-7801
EmailSupport@nexxtspine.com

Device Dimensions

Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree
Length40 Millimeter
Width22 Millimeter
Height14 Millimeter
Angle30 degree

Device Identifiers

Device Issuing AgencyDevice ID
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]
GS100840067206645 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-01-13
Device Publish Date2021-01-05

On-Brand Devices [TrellOss™-L MPF]

0084006720368280-Cell Soft Case, 22mm x 20°
0084006720367580-Cell Soft Case, 18-22mm x 14°
0084006720366880-Cell Soft Case, 18-22mm x 8°
0084006720365180-Cell Soft Case, 18-22mm x 0°
00840067204450Lateral 60Lx22Wx14H 0°
00840067204443Lateral 60Lx22Wx12H 0°
00840067204436Lateral 60Lx22Wx10H 0°
00840067204429Lateral 60Lx22Wx8H 0°
00840067204412Lateral 55Lx22Wx14H 0°
00840067204405Lateral 55Lx22Wx12H 0°
00840067204399Lateral 55Lx22Wx10H 0°
00840067204382Lateral 55Lx22Wx8H 0°
00840067204375Lateral 50Lx22Wx14H 0°
00840067204368Lateral 50Lx22Wx12H 0°
00840067204351Lateral 50Lx22Wx10H 0°
00840067204344Lateral 50Lx22Wx8H 0°
00840067204337Lateral 45Lx22Wx12H 0°
00840067204320Lateral 45Lx22Wx10H 0°
00840067204313Lateral 45Lx22Wx8H 0°
00840067204306Lateral 60Lx18W14H 0°
00840067204290Lateral 60Lx18W12H 0°
00840067204283Lateral 60Lx18W10H 0°
00840067204276Lateral 60Lx18Wx8H 0°
00840067204269Lateral 55Lx18Wx14H 0°
00840067204252Lateral 55Lx18Wx12H 0°
00840067204245Lateral 55Lx18Wx10H 0°
00840067204238Lateral 55Lx18Wx8H 0°
00840067204221Lateral 50Lx18Wx14H 0°
00840067204214Lateral 50Lx18Wx12H 0°
00840067204207Lateral 50Lx18Wx10H 0°
00840067204191Lateral 50Lx18Wx8H 0°
00840067204184Lateral 45Lx18Wx12H 0°
00840067204177Lateral 45Lx18Wx10H 0°
00840067204160Lateral 45Lx18Wx8H 0°
00840067204153Lateral 60Lx22Wx16H 14°
00840067204146Lateral 60Lx22Wx14H 14°
00840067204139Lateral 60Lx22Wx12H 14°
00840067204122Lateral 60Lx22Wx10H 14°
00840067204115Lateral 55Lx22Wx16H 14°
00840067204108Lateral 55Lx22Wx14H 14°
00840067204092Lateral 55Lx22Wx12H 14°
00840067204085Lateral 55Lx22Wx10H 14°
00840067204078Lateral 50Lx22Wx16H 14°
00840067204061Lateral 50Lx22Wx14H 14°
00840067204054Lateral 50Lx22Wx12H 14°
00840067204047Lateral 50Lx22Wx10H 14°
00840067204030Lateral 45Lx22Wx14H 14°
00840067204023Lateral 45Lx22Wx12H 14°
00840067204016Lateral 45Lx22Wx10H 14°
00840067204009TrellOss-L Cage Inserter

Trademark Results [TrellOss]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TRELLOSS
TRELLOSS
88401530 not registered Live/Pending
Zimmer Biomet Spine, Inc.
2019-04-25

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