KNOTILUS+ 3911-600-501

GUDID 07613327623727

CROWN TIP GUIDE

STRYKER CORPORATION

Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable
Primary Device ID07613327623727
NIH Device Record Key9a9965a5-3e69-4827-9e14-0146b67a484c
Commercial Distribution StatusIn Commercial Distribution
Brand NameKNOTILUS+
Version Model Number3911600501
Catalog Number3911-600-501
Company DUNS187502109
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 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+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx
Phone+1(866)624-4422
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327623727 [Primary]

FDA Product Code

FZXGuide, surgical, instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


[07613327623727]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-12-07
Device Publish Date2023-11-29

On-Brand Devices [KNOTILUS+]

07613327623826PENCIL TIP OBTURATOR
07613327623819OFFSET TIP GUIDE
07613327623758FISHMOUTH TIP GUIDE
07613327623734FORK TIP GUIDE, HIP
07613327623727CROWN TIP GUIDE
07613327623710BULLET TIP OBTURATOR, CANNULATED
07613327623680PENCIL TIP OBTURATOR, HIP
07613327623666CROWN TIP GUIDE, HIP
07613327623659BULLET TIP OBTURATOR, CANNULATED, HIP
076133276276572.9X12.5MM KNOTILUS+ ANCHOR - PEEK
076133276276402.9X15.5MM KNOTILUS+ ANCHOR - PEEK
076133276276332.4X11.3MM KNOTILUS+ ANCHOR - PEEK
076133276238332.4X8.9MM DRILL, HARD BONE, HIP
076133276237962.4X8.9MM DRILL, HIP
076133276277012.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK
076133276276642.9X12.5MM KNOTILUS+ HIP ANCHOR - PEEK

Trademark Results [KNOTILUS+]

Mark Image

Registration | Serial
Company
Trademark
Application Date
KNOTILUS+
KNOTILUS+
97615604 not registered Live/Pending
Stryker Corporation
2022-09-30

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