0606100000

GUDID 07613154259793

Friction Cement Gun

STRYKER CORPORATION

Orthopaedic cement/bone filler dispensing gun
Primary Device ID07613154259793
NIH Device Record Key89de6a74-fbd9-4fb5-8ae1-47682dab318c
Commercial Distribution StatusIn Commercial Distribution
Version Model Number0606100000
Catalog Number0606100000
Company DUNS196548481
Company NameSTRYKER CORPORATION
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 Batchfalse
Serial Numbertrue
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+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107613154259793 [Primary]

FDA Product Code

JDZMIXER, CEMENT, FOR CLINICAL USE
KIHDISPENSER, CEMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


[07613154259793]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-02-07
Device Publish Date2018-09-24

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