FDA.reportPublic FDA data

DUALX LLIF 9-12MM x 7 DEG x 60MM

Primary DI
B707128310070100
Brand
DUALX LLIF 9-12MM x 7 DEG x 60MM
Company
AMPLIFY SURGICAL, INC.
Model
12831007010
Device description
LLIF IMPLANT - 7° x 22MM IMPLANTSLordosis & Heights: 9-12mm x 7° x 60mmCollapsed Width (mm): 13.34Expanded Width (mm): 22Collapsed Height (mm): 9.5Expanded Height (mm): 12.5Collapsed Length (mm): 68.76Expanded Length (mm): 61.8
Published
2019-07-25
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

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
K181397000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K181397000DualXInnovasive, Inc.2018-09-27MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B707128310070100PrimaryHIBCC0

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.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
7652675439udi@amplifysurgical.com

Regulatory Flags#

DUNS number
081021000
Device count
1
Lot or batch
true
Expiration date on label
true
No natural rubber latex
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
B70712535005S0Dual X Graft Tamp Short12535005S2026-05-27
B707129410010130DUALXS T/PLIF 15 DEG x 9-12MM129410010132026-05-27
B707129410010200DUALXS T/PLIF 18 DEG x 10-13MM129410010202026-05-27
B707125355740300DUALX DUAL PORTAL DISPOSABLE KIT-30MM (USA)125355740302026-03-05
B707125355740400DUALX DUAL PORTAL DISPOSABLE KIT-40MM (USA)125355740402026-03-05
B707125355740500DUALX DUAL PORTAL DISPOSABLE KIT-50MM (USA)125355740502026-03-05
B707125355740600DUALX DUAL PORTAL DISPOSABLE KIT-60MM (USA)125355740602026-03-05
B707125355740700DUALX DUAL PORTAL DISPOSABLE KIT-70MM (USA)125355740702026-03-05
B707125355740800DUALX DUAL PORTAL DISPOSABLE KIT-80MM (USA)125355740802026-03-05
B707125355740900DUALX DUAL PORTAL DISPOSABLE KIT-90MM (USA)125355740902026-03-05
B707125355741000DUALX DUAL PORTAL DISPOSABLE KIT-100MM (USA)125355741002026-03-05
B707125355741100DUALX DUAL PORTAL DISPOSABLE KIT-110MM (USA)125355741102026-03-05
B707125355741200DUALX DUAL PORTAL DISPOSABLE KIT-120MM (USA)125355741202026-03-05
B707125355860DUALX DUAL PORT HEMOSTATIC AGENT DELIVERY TUBE (USA)125355862025-05-29
B70712535588001US0DUALX DUAL PORT CANNULA 30MM12535588001US2025-05-29
B70712535588002US0DUALX DUAL PORT CANNULA 40MM12535588002US2025-05-29
B70712535588003US0DUALX DUAL PORT CANNULA 50MM12535588003US2025-05-29
B70712535588004US0DUALX DUAL PORT CANNULA 60MM12535588004US2025-05-29
B70712535588005US0DUALX DUAL PORT CANNULA 70MM12535588005US2025-05-29
B70712535588006US0DUALX DUAL PORTAL CANNULA 80MM12535588006US2025-05-29

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Primary DI, Brand, Company table
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