Nuffield Total Knee 117.304

GUDID 05055196910003

NTK PATELLA

CORIN LTD

Polyethylene patella prosthesis Polyethylene patella prosthesis Polyethylene patella prosthesis Polyethylene patella prosthesis Polyethylene patella prosthesis Polyethylene patella prosthesis Polyethylene patella prosthesis Polyethylene patella prosthesis Polyethylene patella prosthesis Polyethylene patella prosthesis
Primary Device ID05055196910003
NIH Device Record Keyd56ce594-0baf-40b1-9c4e-6249e18e3d24
Commercial Distribution StatusIn Commercial Distribution
Brand NameNuffield Total Knee
Version Model Number117.304
Catalog Number117.304
Company DUNS295437313
Company NameCORIN LTD
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+441285659866
Emaillucinda.gerber@coringroup.com
Phone+441285659866
Emaillucinda.gerber@coringroup.com
Phone+441285659866
Emaillucinda.gerber@coringroup.com
Phone+441285659866
Emaillucinda.gerber@coringroup.com
Phone+441285659866
Emaillucinda.gerber@coringroup.com
Phone+441285659866
Emaillucinda.gerber@coringroup.com
Phone+441285659866
Emaillucinda.gerber@coringroup.com
Phone+441285659866
Emaillucinda.gerber@coringroup.com
Phone+441285659866
Emaillucinda.gerber@coringroup.com
Phone+441285659866
Emaillucinda.gerber@coringroup.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105055196910003 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[05055196910003]

Radiation Sterilization

[05055196910003]

Radiation Sterilization

[05055196910003]

Radiation Sterilization

[05055196910003]

Radiation Sterilization

[05055196910003]

Radiation Sterilization

[05055196910003]

Radiation Sterilization

[05055196910003]

Radiation Sterilization

[05055196910003]

Radiation Sterilization

[05055196910003]

Radiation Sterilization

[05055196910003]

Radiation Sterilization

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-08-17

On-Brand Devices [Nuffield Total Knee]

05055343893630NTK
05055196946262NTK STEMLESS FEMUR
05055196946095NTK TIBIA LONG STEM
05055196946088NTK TIBIA LONG STEM
05055196946071NTK TIBIA LONG STEM
05055196946057NTK STEMLESS FEMUR
05055196945982NTK STEM FEMUR
05055196945975NTK STEM FEMUR
05055196945968NTK STEM FEMUR
05055196945951NTK STEM FEMUR
05055196945944NTK STEM FEMUR
05055196945838NTK STEM FEMUR
05055196945821NTK STEM FEMUR
05055196945814NTK STEM FEMUR
05055196945807NTK STEM FEMUR
05055196945791NTK STEM FEMUR
05055196913387NTK TIBIA INSERT
05055196913370NTK TIBIA INSERT
05055196913363NTK TIBIA INSERT
05055196913356NTK TIBIA INSERT
05055196913349NTK TIBIA INSERT
05055196913325NTK TIBIA INSERT
05055196913318NTK TIBIA INSERT
05055196913301NTK TIBIA INSERT
05055196913288NTK TIBIA INSERT
05055196913271NTK TIBIA INSERT
05055196913264NTK TIBIA INSERT
05055196913257NTK TIBIA INSERT
05055196910744NTK TIBIA STD STEM
05055196910737NTK TIBIA STD STEM
05055196910720NTK TIBIA STD STEM
05055196910713NTK TIBIA STD STEM
05055196910706NTK TIBIA STD STEM
05055196910010NTK PATELLA
05055196910003NTK PATELLA
05055196909847NTK PEGGED FEMUR
05055196909830NTK PEGGED FEMUR
05055196909823NTK PEGGED FEMUR
05055196909816NTK PEGGED FEMUR
05055196909809NTK PEGGED FEMUR
05055196909793NTK PEGGED FEMUR
05055196909786NTK PEGGED FEMUR
05055196909779NTK PEGGED FEMUR
05055196909762NTK PEGGED FEMUR
05055196909755NTK PEGGED FEMUR
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