MectaLIF 3D

Primary DI
07630542743085
Brand
MectaLIF 3D
Company
Medacta International SA
Model
03.44.042
Device description
MectaLIF Oblique Dome 3D 10x40x12
Published
2025-07-25
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
K251016000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K251016000MectaLIF 3D MetalMedacta International S.A.2025-07-17MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07630542743085PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07630542743085076305427430857630542743085

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 typically in the form of a hollow, porous, threaded and/or fenestrated cylindrical, or disc-shaped 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 packaged with the cage.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
488227125
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
07630542762482GMK Extension02.12.0110APFL2026-09-18
07630542762499GMK Extension02.12.0110APFR2026-09-18
07630542762505GMK Extension02.12.0111APFL2026-09-18
07630542762512GMK Extension02.12.0111APFR2026-09-18
07630542762529GMK Extension02.12.0112APFL2026-09-18
07630542762536GMK Extension02.12.0112APFR2026-09-18
07630542762543GMK Extension02.12.0113APFL2026-09-18
07630542762550GMK Extension02.12.0113APFR2026-09-18
07630542762567GMK Extension02.12.0114APFL2026-09-18
07630542762574GMK Extension02.12.0114APFR2026-09-18
07630542762581GMK Extension02.12.0117APFL2026-09-18
07630542762598GMK Extension02.12.0117APFR2026-09-18
07630542762604GMK Extension02.12.0120APFL2026-09-18
07630542762611GMK Extension02.12.0120APFR2026-09-18
07630542762628GMK Extension02.12.0210APFL2026-09-18
07630542762635GMK Extension02.12.0210APFR2026-09-18
07630542762642GMK Extension02.12.0211APFL2026-09-18
07630542762659GMK Extension02.12.0211APFR2026-09-18
07630542762666GMK Extension02.12.0212APFL2026-09-18
07630542762673GMK Extension02.12.0212APFR2026-09-18

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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B707125355730600DUALX DUAL PORTAL DISPOSABLE KIT-60MM (USA)AMPLIFY SURGICAL, INC.MAX2026-09-04
B707125355730700DUALX DUAL PORTAL DISPOSABLE KIT-70MM (USA)AMPLIFY SURGICAL, INC.MAX2026-09-04
B707125355730800DUALX DUAL PORTAL DISPOSABLE KIT-80MM (USA)AMPLIFY SURGICAL, INC.MAX2026-09-04
B707125355730900DUALX DUAL PORTAL DISPOSABLE KIT-90MM (USA)AMPLIFY SURGICAL, INC.MAX2026-09-04
B707125355731000DUALX DUAL PORTAL DISPOSABLE KIT-100MM (USA)AMPLIFY SURGICAL, INC.MAX2026-09-04
B707125355731100DUALX DUAL PORTAL DISPOSABLE KIT-110MM (USA)AMPLIFY SURGICAL, INC.MAX2026-09-04
B707125355731200DUALX DUAL PORTAL DISPOSABLE KIT-120MM (USA)AMPLIFY SURGICAL, INC.MAX2026-09-04
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