Avenue T AT0025P

GUDID 03662663001656

Avenue T Cage H14mm L30mm 5°

LDR Spine Usa, Inc.

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Primary Device ID03662663001656
NIH Device Record Key9a4c72b4-26f2-4dd2-86b1-f3a4da1b4993
Commercial Distribution StatusIn Commercial Distribution
Brand NameAvenue T
Version Model NumberAT0025P
Catalog NumberAT0025P
Company DUNS615789729
Company NameLDR Spine Usa, 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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com

Device Dimensions

Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree
Height14 Millimeter
Length30 Millimeter
Angle5 degree

Device Identifiers

Device Issuing AgencyDevice ID
GS103662663001656 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OVDIntervertebral Fusion Device With Integrated Fixation, Lumbar

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2022-03-10
Device Publish Date2017-04-12

On-Brand Devices [Avenue T]

03662663002882CAGE HOLDER
03662663026024AT990D
03662663026017AT990C
03662663023696AT990B
03662663023689AT990A
03662663024273TRIAL H19MM 9°
03662663024266TRIAL H18MM 9°
03662663024259TRIAL H17MM 9°
03662663024242TRIAL H16MM 9°
03662663024235TRIAL H15MM 9°
03662663024228TRIAL H14MM 9°
03662663024211TRIAL H13MM 9°
03662663024204TRIAL H12MM 9°
03662663024198TRIAL H11MM 9°
03662663024181TRIAL H17MM 5°
03662663024174TRIAL H16MM 5°
03662663024167TRIAL H15MM 5°
03662663024150TRIAL H14MM 5°
03662663024143TRIAL H13MM 5°
03662663024136TRIAL H12MM 5°
03662663024129TRIAL H11MM 5°
03662663024112TRIAL H10MM 5°
03662663024105TRIAL H14MM 0°
03662663024099TRIAL H13MM 0°
03662663024082TRIAL H12MM 0°
03662663024075TRIAL H11MM 0°
03662663024068TRIAL H10MM 0°
03662663024051TRIAL H9MM 0°
03662663024044TRIAL H8MM 0°
03662663024037TRIAL H7,5MM 0°
03662663023672AVENUE T ANCHORING PLATE "L"
03662663023665AVENUE T ANCHORING PLATE "M"
03662663023658AVENUE T ANCHORING PLATE "S"
03662663003070AT9044R
03662663003063AT9043R
03662663003056AT9041R
03662663003049AT9040R
03662663003032AT9039R
03662663003025AT9038R
03662663003018AT9037R
03662663002936AT9042R
03662663002912DOUBLE IMPACTOR
03662663002899IMPACTOR
03662663002875AT9031R
03662663002868AT9030R
03662663002851AT9029R
03662663002844AT9028R
03662663002837AT9027R
03662663002820AT9026R
03662663002813AT9025R

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