K2M Fenestrated Tap System 5001-90011

GUDID 10888857183087

Fenestrated Tap Adapter Quick Connect

K2M, INC.

Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID10888857183087
NIH Device Record Key6f36d52e-102c-4403-b9b3-49a0e55cedb4
Commercial Distribution StatusIn Commercial Distribution
Brand NameK2M Fenestrated Tap System
Version Model Number5001-90011
Catalog Number5001-90011
Company DUNS146060863
Company NameK2M, 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+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com
Phone+1(571)919-2000
Emailmark.zellers@stryker.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110888857183087 [Primary]

FDA Product Code

LXHOrthopedic manual surgical instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


[10888857183087]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-15
Device Publish Date2022-08-06

On-Brand Devices [K2M Fenestrated Tap System]

10888857183148Tap, Fenestrated, Size Ø8.5 mm
10888857183131Tap, Fenestrated, Size Ø7.5 mm
10888857183124Tap, Fenestrated, Size Ø6.5 mm
10888857183117Tap, Fenestrated, Size Ø5.5 mm
10888857183100Tap, Fenestrated, Size Ø4.5 mm
10888857183094Tap, Fenestrated, Size Ø4.0 mm
10888857461338Tap, Fenestrated, Size Ø8.5
10888857461321Tap, Fenestrated, Size Ø7.5
10888857461314Tap, Fenestrated, Size Ø6.5
10888857461307Tap, Fenestrated, Size Ø5.5
10888857461291Tap, Fenestrated, Size Ø4.5
10888857461284Tap, Fenestrated, Size Ø3.5
10888857530096Tap, Fenestrated Size Ø8.5
10888857530089Tap, Fenestrated Size Ø7.5
10888857530072Tap, Fenestrated Size Ø6.5
10888857530065Tap, Fenestrated Size Ø5.5
10888857530058Tap, Fenestrated Size Ø4.5
10888857530041Tap, Fenestrated Size Ø4.0
10888857183087Fenestrated Tap Adapter Quick Connect

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