FDA.reportPublic FDA data

EZ-Track

Primary DI
00840314101709
Brand
EZ-Track
Company
NEXT ORTHOSURGICAL, INC.
Model
CABB300907A
Catalog number
CABB300907A
Device description
OTLIF INTERBODY CAGE, 9 X 30 X 7MM -0°
Published
2024-08-14
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Product Codes#

Code, Name table
CodeName
MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K131082000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K131082000INTERFORM INTERBODY CAGE SYSTEMNext Orthosurgical2013-08-26MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00840314101709PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00840314101709008403141017098403141017090840314101709

GMDN Terms#

Term, Definition table
TermDefinition
Polymeric 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 non-bioabsorbable synthetic polymer [e.g., polyetheretherketone (PEEK)] 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.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
046767258
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00840314141798Nex-D2CBCAJ-10000CBCAJ-100002024-09-16
00840314141804Nex-D2CBCBJ-10000CBCBJ-100002024-09-16
00840314165923Nex-D2CBFBJ-70140CBFBJ-701402024-09-05
00840314165930Nex-D2CBFBJ-70145CBFBJ-701452024-09-05
00840314165947Nex-D2CBFBJ-70150CBFBJ-701502024-09-05
00840314165954Nex-D2CBFBJ-78020CBFBJ-780202024-09-05
00840314165961Nex-D2CBFBJ-78025CBFBJ-780252024-09-05
00840314165978Nex-D2CBFBJ-78030CBFBJ-780302024-09-05
00840314165985Nex-D2CBFBJ-78035CBFBJ-780352024-09-05
00840314165992Nex-D2CBFBJ-78040CBFBJ-780402024-09-05
00840314166005Nex-D2CBFBJ-78045CBFBJ-780452024-09-05
00840314166012Nex-D2CBFBJ-78050CBFBJ-780502024-09-05
00840314166029Nex-D2CBFBJ-78055CBFBJ-780552024-09-05
00840314166036Nex-D2CBFBJ-78060CBFBJ-780602024-09-05
00840314166043Nex-D2CBFBJ-78065CBFBJ-780652024-09-05
00840314166050Nex-D2CBFBJ-78070CBFBJ-780702024-09-05
00840314166067Nex-D2CBFBJ-78075CBFBJ-780752024-09-05
00840314166074Nex-D2CBFBJ-78080CBFBJ-780802024-09-05
00840314166081Nex-D2CBFBJ-78085CBFBJ-780852024-09-05
00840314166098Nex-D2CBFBJ-78090CBFBJ-780902024-09-05

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00197157075859ZAVATION INSERTERZavation LLCMAX2026-05-27
00810166522366X-PACEXPANDING INNOVATIONS, INC.MAX2026-05-27
00810166522373X-PACEXPANDING INNOVATIONS, INC.MAX2026-05-27
B70712535005S0Dual X Graft Tamp ShortAMPLIFY SURGICAL, INC.MAX2026-05-27
B707129410010130DUALXS T/PLIF 15 DEG x 9-12MMAMPLIFY SURGICAL, INC.MAX2026-05-27
B707129410010200DUALXS T/PLIF 18 DEG x 10-13MMAMPLIFY SURGICAL, INC.MAX2026-05-27
07613153046196AVS PLStryker CorporationMAX2015-09-14
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