FDA.reportPublic FDA data

AccelFix Lumbar Expandable Cage System

Primary DI
08800061635348
Brand
AccelFix Lumbar Expandable Cage System
Company
L&K BIOMED CO. ,LTD.
Model
L6518-0806S
Catalog number
L6518-0806S
Device description
AccelFix-XL, 6°, 65X18X8mm
Published
2019-10-21
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Sterile
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
K190708000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K190708000AccelFix Lumbar Interbody Fusion Cage SystemL&K BIOMED Co., Ltd.2019-09-16MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
08800061635348PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
08800061635348088000616353488800061635348

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

Regulatory Flags#

DUNS number
631159324
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
08809986491008BluEX Cervical Expandable Cage System1417-1000S2026-06-04
08809986491015BluEX Cervical Expandable Cage System1417-1100S2026-06-04
08809986491022BluEX Cervical Expandable Cage System1417-1200S2026-06-04
08809986491039BluEX Cervical Expandable Cage System1417-1300S2026-06-04
08809986491046BluEX Cervical Expandable Cage System1417-0407S2026-06-04
08809986491053BluEX Cervical Expandable Cage System1417-0507S2026-06-04
08809986491060BluEX Cervical Expandable Cage System1417-0607S2026-06-04
08809986491077BluEX Cervical Expandable Cage System1417-0707S2026-06-04
08809986491084BluEX Cervical Expandable Cage System1417-0807S2026-06-04
08809986491091BluEX Cervical Expandable Cage System1417-0907S2026-06-04
08809986491107BluEX Cervical Expandable Cage System1417-1007S2026-06-04
08809986491114BluEX Cervical Expandable Cage System1417-1107S2026-06-04
08809986491121BluEX Cervical Expandable Cage System1417-1207S2026-06-04
08809986491138BluEX Cervical Expandable Cage System1417-1307S2026-06-04
08809986491145CastleLoc-P Anterior Cervical Plate System6911-17152026-06-04
08809986491152CastleLoc-P Anterior Cervical Plate System6911-17172026-06-04
08809986491169CastleLoc-P Anterior Cervical Plate System6911-17192026-06-04
08809986491176CastleLoc-P Anterior Cervical Plate System6911-17212026-06-04
08809986491183CastleLoc-P Anterior Cervical Plate System6911-17232026-06-04
08809986491190CastleLoc-P Anterior Cervical Plate System6911-17252026-06-04

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
08800043912870N/ATDM Co., Ltd.MAX2026-06-02
08800043912887N/ATDM Co., Ltd.MAX2026-06-02
08800043912894N/ATDM Co., Ltd.MAX2026-06-02
08800043912900N/ATDM Co., Ltd.MAX2026-06-02
08800043912917N/ATDM Co., Ltd.MAX2026-06-02
08800043912924N/ATDM Co., Ltd.MAX2026-06-02
08800043912931N/ATDM Co., Ltd.MAX2026-06-02
08800043912948N/ATDM Co., Ltd.MAX2026-06-02
08800043912955N/ATDM Co., Ltd.MAX2026-06-02
08800043912962N/ATDM Co., Ltd.MAX2026-06-02
08800043912979N/ATDM Co., Ltd.MAX2026-06-02
08800043912986N/ATDM Co., Ltd.MAX2026-06-02
08800043912993N/ATDM Co., Ltd.MAX2026-06-02
08800043913006N/ATDM Co., Ltd.MAX2026-06-02
08800043913013N/ATDM Co., Ltd.MAX2026-06-02
08800043913020N/ATDM Co., Ltd.MAX2026-06-02
08800043913037N/ATDM Co., Ltd.MAX2026-06-02
08800043913044N/ATDM Co., Ltd.MAX2026-06-02
08800043913051N/ATDM Co., Ltd.MAX2026-06-02
08800043913068N/ATDM Co., Ltd.MAX2026-06-02
08800043913075N/ATDM Co., Ltd.MAX2026-06-02
08800043964183N/ATDM Co., Ltd.MAX2026-06-02
08800043964190N/ATDM Co., Ltd.MAX2026-06-02
08800043964206N/ATDM Co., Ltd.MAX2026-06-02
08800043964213N/ATDM Co., Ltd.MAX2026-06-02
08800043964220N/ATDM Co., Ltd.MAX2026-06-02
08800043964237N/ATDM Co., Ltd.MAX2026-06-02
08800043964244N/ATDM Co., Ltd.MAX2026-06-02
08800043964251N/ATDM Co., Ltd.MAX2026-06-02
08800043964268N/ATDM Co., Ltd.MAX2026-06-02