SPINAL FUSION CURETTE

GUDID 00192896101807

Spinal Fusion Curette Straight Tip

SONTEC INSTRUMENTS, INC.

Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable Bone curette, reusable
Primary Device ID00192896101807
NIH Device Record Key8939c3ce-46a5-4b22-9427-77ee9daad725
Commercial Distribution StatusIn Commercial Distribution
Brand NameSPINAL FUSION CURETTE
Version Model Number320-867-9-6
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, 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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com
Phone+1(800)821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Device Size Text, specify0
Length9 Inch
Device Size Text, specify0
Length9 Inch
Device Size Text, specify0
Length9 Inch
Device Size Text, specify0
Length9 Inch
Device Size Text, specify0
Length9 Inch
Device Size Text, specify0
Length9 Inch
Device Size Text, specify0
Length9 Inch
Device Size Text, specify0
Length9 Inch
Device Size Text, specify0
Length9 Inch
Device Size Text, specify0
Length9 Inch
Device Size Text, specify0
Length9 Inch

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896101807 [Primary]

FDA Product Code

HTFCURETTE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896101807]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101807]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101807]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101807]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101807]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101807]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101807]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101807]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101807]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101807]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


[00192896101807]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-05-26
Device Publish Date2020-05-18

On-Brand Devices [SPINAL FUSION CURETTE]

00192896077768SPINAL FUSION CURETTE STRAIGHT TIP SIZE 0
00192896101838Spinal Fusion Curette Straight Tip
00192896101821Spinal Fusion Curette Straight Tip
00192896101814Spinal Fusion Curette Straight Tip
00192896101807Spinal Fusion Curette Straight Tip

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