5mm Straight Curette 6189-02

GUDID 81195401235986

INTERVENTIONAL SPINE, INC

Bone curette, reusable
Primary Device ID81195401235986
NIH Device Record Keye9d88e47-7fcf-4245-a046-767e99416a3d
Commercial Distribution Discontinuation2016-12-23
Commercial Distribution StatusNot in Commercial Distribution
Brand Name5mm Straight Curette
Version Model Number6189-02
Catalog Number6189-02
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

Phone800-497-0484
Emailwww.cs@i-spineinc.com
Phone800-497-0484
Emailwww.cs@i-spineinc.com

Device Identifiers

Device Issuing AgencyDevice ID
GS181195401235986 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[81195401235986]

Moist Heat or Steam Sterilization


[81195401235986]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-05-07
Device Publish Date2015-09-21

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