FDA.reportPublic FDA data

TrellOss™

Primary DI
00840067200728
Brand
TrellOss™
Company
NEXXT SPINE, LLC
Model
208M2213
Device description
Straight 22Dx9Wx13H 6°
Published
2019-05-08
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
MAXIntervertebral Fusion Device With Bone Graft, Lumbar
MQPSpinal Vertebral Body Replacement Device

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2
MQPSpinal Vertebral Body Replacement DeviceOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K171140000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K171140000Matrixx SystemNexxt Spine, LLC2017-08-22ODP

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840067200728PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840067200728008400672007288400672007280840067200728

GMDN Terms#

Term, Definition table
TermDefinition
Metallic spinal interbody fusion cageA device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is in the form of a hollow, porous, threaded and/or fenestrated cylindrical or geometrical device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be included with the device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Angle6degree
Height13Millimeter
Length22Millimeter
Width9Millimeter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
317-436-7801Support@nexxtspine.com

Regulatory Flags#

DUNS number
003489810
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00889929060209Inertia® CONNEXX™ Modular Pedicle Screw System20-SCC-85852024-12-18
00889929072400NEXXT MATRIXX® SI SystemC64-01-032026-07-10
00889929072738NEXXT MATRIXX® SI SystemI64-15-082026-05-01
00840067212189TrellOss®-A SA432H00142026-06-24
00840067212196TrellOss®-A SA432H00192026-06-24
00840067212202TrellOss®-A SA432H00202026-06-24
00840067212219TrellOss®-A SA432H00212026-06-24
00840067212226TrellOss®-A SA432H00222026-06-24
00840067212233TrellOss®-A SA432H00232026-06-24
00840067212240TrellOss®-A SA432H00242026-06-24
00840067212257TrellOss®-A SA432H01082026-06-24
00840067212264TrellOss®-A SA432H01102026-06-24
00840067212271TrellOss®-A SA432H01122026-06-24
00840067212288TrellOss®-A SA432H01142026-06-24
00840067212295TrellOss®-A SA432H01162026-06-24
00840067212301TrellOss®-A SA432H01182026-06-24
00840067212318TrellOss®-A SA432H01202026-06-24
00889929072752NEXXT MATRIXX® Stand Alone ALIF SystemI61-03-022026-06-24
00889929072769NEXXT MATRIXX® Stand Alone ALIF SystemI61-20-072026-06-24
00889929072776NEXXT MATRIXX® Stand Alone ALIF SystemI61-20-082026-06-24

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
M719GLL100QC03DP Lumbar Interbody SystemGenesys Orthopedics Systems LLCMAX2026-07-14
M719GLL101QC03DP Lumbar Interbody SystemGenesys Orthopedics Systems LLCMAX2026-07-14
M719GLL106QC03DP Lumbar Interbody SystemGenesys Orthopedics Systems LLCMAX2026-07-14
M719GLL107QC03DP Lumbar Interbody SystemGenesys Orthopedics Systems LLCMAX2026-07-14
00763000857820T2 STRATOSPHERE™ Expandable Corpectomy SystemMEDTRONIC SOFAMOR DANEK, INC.MQP2026-06-26
00763000858001T2 STRATOSPHERE™ Expandable Corpectomy SystemMEDTRONIC SOFAMOR DANEK, INC.MQP2026-06-26
08800043913099N/ATDM Co., Ltd.MAX2026-06-10
08800043913105N/ATDM Co., Ltd.MAX2026-06-10
08800043913112N/ATDM Co., Ltd.MAX2026-06-10
08800043913129N/ATDM Co., Ltd.MAX2026-06-10
08800043913136N/ATDM Co., Ltd.MAX2026-06-10
08800043913143N/ATDM Co., Ltd.MAX2026-06-10
08800043913150N/ATDM Co., Ltd.MAX2026-06-10
08800043913167N/ATDM Co., Ltd.MAX2026-06-10
08800043913174N/ATDM Co., Ltd.MAX2026-06-10
08800043913181N/ATDM Co., Ltd.MAX2026-06-10
08800043913198N/ATDM Co., Ltd.MAX2026-06-10
08800043913204N/ATDM Co., Ltd.MAX2026-06-10
08800043913211N/ATDM Co., Ltd.MAX2026-06-10
08800043917288N/ATDM Co., Ltd.MAX2026-06-10
08800043917295N/ATDM Co., Ltd.MAX2026-06-10
08800043917301N/ATDM Co., Ltd.MAX2026-06-10
00887517729545TLXNuvasive, Inc.MAX2026-04-25
00887517729576TLXNuvasive, Inc.MAX2026-04-25
00887517729620TLXNuvasive, Inc.MAX2026-04-25
00887517729644TLXNuvasive, Inc.MAX2026-04-25
00887517729705TLXNuvasive, Inc.MAX2026-04-25
00887517729767TLXNuvasive, Inc.MAX2026-04-25
00887517729781TLXNuvasive, Inc.MAX2026-04-25
00887517824912TLXNuvasive, Inc.MAX2026-04-25