7.3mm Pull Pin Remover 6039

GUDID 00811954012991

INTERVENTIONAL SPINE, INC

Orthopaedic implant inserter/extractor, reusable
Primary Device ID00811954012991
NIH Device Record Keyf88e048d-411a-4c43-81aa-6373c6edd538
Commercial Distribution StatusIn Commercial Distribution
Brand Name7.3mm Pull Pin Remover
Version Model Number6039
Catalog Number6039
Company DUNS017663522
Company NameINTERVENTIONAL SPINE, INC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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

Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com
Phone(800)497-0484
Emailwww.cs@i-spineinc.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100811954012991 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


[00811954012991]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-04-23
Device Publish Date2015-12-22

Devices Manufactured by INTERVENTIONAL SPINE, INC

00011954013448 - 8 Degree Lordotic, Opticage Expandable Interbody Implant2020-02-24 22mm Width x 45mm Length by 11mm-16mm Footprint Length
81195401082986 - Opticage Expandable Interbody Implant2020-02-24 9mm Width x 21mm Length by 9mm-14mm Expandable Height
81195401107962 - Opticage Expandable Interbody Implant2020-02-24 9mm Width x 26mm Length by 9mm-14mm Expandable Height
81195401108648 - Opticage Expandable Interbody Implant2020-02-24 9mm Width x 30mm Length by 9mm-14mm Expandable Height
81195401109393 - Opticage Expandable Interbody Implant2020-02-24 10mm Width x 21mm Length by 9mm-14mm Expandable Height
81195401110900 - Opticage Expandable Interbody Implant2020-02-24 10mm Width x 26mm Length by 9mm-14mm Expandable Height
81195401111686 - Opticage Expandable Interbody Implant2020-02-24 10mm Width x 30mm Length by 9mm-14mm Expandable Height
81195401112362 - Opticage Expandable Interbody Implant2020-02-24 11mm Width x 21mm Length by 9mm-14mm Expandable Height

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