DUALX DUAL PORTAL ROOT RETRACTOR

GUDID B707NHN23020

ROOT RETRACTOR

Amplify Surgical, Inc.

Orthopaedic implant inserter/extractor, reusable
Primary Device IDB707NHN23020
NIH Device Record Keyb1dcde4f-c17b-45b0-8069-43f8380ecb46
Commercial Distribution StatusIn Commercial Distribution
Brand NameDUALX DUAL PORTAL ROOT RETRACTOR
Version Model NumberNHN2302
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
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
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
HIBCCB707NHN23020 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


[B707NHN23020]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-01-23
Device Publish Date2024-01-15

On-Brand Devices [DUALX DUAL PORTAL ROOT RETRACTOR]

B707NHN20020ROOT RETRACTOR
B707NHN19020ROOT RETRACTOR
B707NHN23020ROOT RETRACTOR

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