DUALXS T/PLIF 15 DEG x 8-11MM

GUDID B707129410010120

Lordosis & Heights: 15° x 8-11mm Collapsed Width (mm): 10 Expanded Width (mm): 20 Collapsed Height (mm): 8 Expanded Height (mm): 11

Amplify Surgical, Inc.

Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage Metallic spinal interbody fusion cage
Primary Device IDB707129410010120
NIH Device Record Key81de0a46-db2a-4ce2-b84c-ac4cb906220c
Commercial Distribution StatusIn Commercial Distribution
Brand NameDUALXS T/PLIF 15 DEG x 8-11MM
Version Model Number12941001012
Company DUNS081021000
Company NameAmplify Surgical, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB707129410010120 [Primary]

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


[B707129410010120]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-06-28
Device Publish Date2024-06-20

On-Brand Devices [DUALXS T/PLIF 15 DEG x 8-11MM]

B707129410010060Lordosis & Heights: 15° x 8-11mm Collapsed Width (mm): 10 Expanded Width (mm): 20 Collapsed Hei
B707129410010120Lordosis & Heights: 15° x 8-11mm Collapsed Width (mm): 10 Expanded Width (mm): 20 Collapsed Hei

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