FDA.reportPublic FDA data

GoLIF! Lumbar Interbody Fusion System

Primary DI
07640387660393
Brand
GoLIF! Lumbar Interbody Fusion System
Company
GetSet Surgical SA
Model
3102613
Device description
GoLIF! Lumbar Interbody Fusion Device, 1 PEEK polymers cage 26mm x 13mm
Published
2025-04-01
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
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
K250186000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K250186000GoLIF! Lumbar Interbody Fusion SystemGetset Surgical, SA2025-03-21MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07640387660393PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07640387660393076403876603937640387660393

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
480143831
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
07640387660140GoPLF! Posterior Lateral Fusion Device31000102023-12-12
07640387660003GoPLF! Posterior Lateral Fusion Device32055352022-02-21
07640387660010GoPLF! Posterior Lateral Fusion Device32055402022-02-21
07640387660027GoPLF! Posterior Lateral Fusion Device32055452022-02-21
07640387660034GoPLF! Posterior Lateral Fusion Device32055502022-02-21
07640387660041GoPLF! Posterior Lateral Fusion Device32065352022-02-21
07640387660058GoPLF! Posterior Lateral Fusion Device32065402022-02-21
07640387660065GoPLF! Posterior Lateral Fusion Device32065452023-12-12
07640387660072GoPLF! Posterior Lateral Fusion Device32065502023-12-12
07640387660089GoPLF! Posterior Lateral Fusion Device32065552023-12-12
07640387660096GoPLF! Posterior Lateral Fusion Device32075352023-12-12
07640387660102GoPLF! Posterior Lateral Fusion Device32075402023-12-12
07640387660119GoPLF! Posterior Lateral Fusion Device32075452023-12-12
07640387660126GoPLF! Posterior Lateral Fusion Device32075502023-12-12
07640387660133GoPLF! Posterior Lateral Fusion Device32075552023-12-12
07640387660157GoPLF! Posterior Lateral Fusion Device32000352023-12-12
07640387660164GoPLF! Posterior Lateral Fusion Device32000402023-12-12
07640387660171GoPLF! Posterior Lateral Fusion Device32000452023-12-12
07640387660188GoPLF! Posterior Lateral Fusion Device32000502023-12-12
07640387660195GoPLF! Posterior Lateral Fusion Device32000552023-12-12

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Primary DI, Brand, Company table
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00840606196031VertuSPINAL ELEMENTS, INC.MAX2026-09-25
00840606196048VertuSPINAL ELEMENTS, INC.MAX2026-09-25
00810017915170SABER-XA, Screw Ø5.5 x 32.5ELEVATION SPINE, INC.MAX2026-09-22
10888857461819CASCADIA™ Interbody SystemVB Spine LLCMAX2019-10-31
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