VerteFIT VF9109R

GUDID 03662663033206

LDR Spine Usa, Inc.

Orthopaedic surgical distractor, internal
Primary Device ID03662663033206
NIH Device Record Key0b618351-a71c-48c8-9b54-d0536dfd170b
Commercial Distribution StatusIn Commercial Distribution
Brand NameVerteFIT
Version Model NumberVF9109R
Catalog NumberVF9109R
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
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
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 Identifiers

Device Issuing AgencyDevice ID
GS103662663033206 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQPSpinal Vertebral Body Replacement Device

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


[03662663033206]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-03-10
Device Publish Date2018-12-12

On-Brand Devices [VerteFIT]

03662663033282VF9117R
03662663033275VF9116R
03662663033114VF9012R
03662663036184VF3102T
03662663036177VF2102T
03662663036160VF1102T
03662663049290VF991C-CR
03662663049283VF991B-CR
03662663049276VF991A-CR
03662663049238VF990-CR
03662663036153VF9192R
03662663036146VF9191R
03662663036139VF9190R
03662663035422VF9118R
03662663035170VF9013R
03662663033268VF9115R
03662663033213VF9110R
03662663033206VF9109R
03662663033190VF9108R
03662663033183VF9107R
03662663033107VF9011R
03662663033077VF9008R
03662663033060VF9007R
03662663033053VerteFIT

Trademark Results [VerteFIT]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VERTEFIT
VERTEFIT
86539376 not registered Dead/Abandoned
LDR Medical, S.A.S.
2015-02-19

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.