Columbus® CR NN930K

GUDID 04046963361983

COLUMBUS CR NARROW FEMUR PLASMAP.F5N R

Aesculap AG

Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis Coated knee femur prosthesis
Primary Device ID04046963361983
NIH Device Record Key0c4500a1-bdda-48f9-972b-5f6465fa14ef
Commercial Distribution StatusIn Commercial Distribution
Brand NameColumbus® CR
Version Model NumberNN930K
Catalog NumberNN930K
Company DUNS315018218
Company NameAesculap AG
Device Count1
DM Exemptfalse
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+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com
Phone+1(888)229-3002
Emailsetworld_orders@aesculap.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]
GS104046963361983 [Primary]

FDA Product Code

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

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-07-30
Device Publish Date2015-09-24

On-Brand Devices [Columbus® CR]

04038653351367COLUMBUS CR FEMORAL COMP.CEMENTED F4L
04038653351343COLUMBUS CR FEMORAL COMP.CEMENTED F2L
04038653351336COLUMBUS CR FEMORAL COMP.CEMENTED F1L
04046963001506COLUMBUS CR FEMORAL COMP.PLASMAPORE F8R
04046963001490COLUMBUS CR FEMORAL COMP.PLASMAPORE F8L
04038653351688COLUMBUS CR FEMORAL COMP.PLASMAPORE F6R
04038653351671COLUMBUS CR FEMORAL COMP.PLASMAPORE F5R
04038653351664COLUMBUS CR FEMORAL COMP.PLASMAPORE F4R
04038653351657COLUMBUS CR FEMORAL COMP.PLASMAPORE F3R
04038653351640COLUMBUS CR FEMORAL COMP.PLASMAPORE F2R
04038653351633COLUMBUS CR FEMORAL COMP.PLASMAPORE F1R
04038653351626COLUMBUS CR FEMORAL COMP.PLASMAPORE F7L
04038653351619COLUMBUS CR FEMORAL COMP.PLASMAPORE F6L
04038653351602COLUMBUS CR FEMORAL COMP.PLASMAPORE F5L
04038653351596COLUMBUS CR FEMORAL COMP.PLASMAPORE F4L
04038653351589COLUMBUS CR FEMORAL COMP.PLASMAPORE F3L
04038653351572COLUMBUS CR FEMORAL COMP.PLASMAPORE F2L
04038653351565COLUMBUS CR FEMORAL COMP.PLASMAPORE F1L
04038653351480COLUMBUS CR FEMORAL COMP.CEMENTED F8R
04038653351473COLUMBUS CR FEMORAL COMP.CEMENTED F7R
04038653351466COLUMBUS CR FEMORAL COMP.CEMENTED F6R
04038653351459COLUMBUS CR FEMORAL COMP.CEMENTED F5R
04038653351435COLUMBUS CR FEMORAL COMP.CEMENTED F3R
04038653351428COLUMBUS CR FEMORAL COMP.CEMENTED F2R
04038653351411COLUMBUS CR FEMORAL COMP.CEMENTED F1R
04038653351404COLUMBUS CR FEMORAL COMP.CEMENTED F8L
04038653351398COLUMBUS CR FEMORAL COMP.CEMENTED F7L
04038653351381COLUMBUS CR FEMORAL COMP.CEMENTED F6L
04038653351374COLUMBUS CR FEMORAL COMP.CEMENTED F5L
04046963429140COLUMBUS CR NARROW FEMUR CEMENTED F3N R
04046963429133COLUMBUS CR NARROW FEMUR CEMENTED F2N R
04046963429126COLUMBUS CR NARROW FEMUR CEMENTED F3N L
04046963429119COLUMBUS CR NARROW FEMUR CEMENTED F2N L
04046963361860COLUMBUS CR NARROW FEMUR CEMENTED F6N R
04046963361853COLUMBUS CR NARROW FEMUR CEMENTED F5N R
04046963361846COLUMBUS CR NARROW FEMUR CEMENTED F4N R
04046963361839COLUMBUS CR NARROW FEMUR CEMENTED F6N L
04046963361822COLUMBUS CR NARROW FEMUR CEMENTED F5N L
04046963361815COLUMBUS CR NARROW FEMUR CEMENTED F4N L
04038653351442COLUMBUS CR FEMORAL COMP.CEMENTED F4R
04046963429270COLUMBUS CR NARROW FEMUR PLASMAP.F3N R
04046963429232COLUMBUS CR NARROW FEMUR PLASMAP.F2N R
04046963429195COLUMBUS CR NARROW FEMUR PLASMAP.F3N L
04046963429188COLUMBUS CR NARROW FEMUR PLASMAP.F2N L
04046963361990COLUMBUS CR NARROW FEMUR PLASMAP.F6N R
04046963361983COLUMBUS CR NARROW FEMUR PLASMAP.F5N R
04046963361976COLUMBUS CR NARROW FEMUR PLASMAP.F4N R
04046963361969COLUMBUS CR NARROW FEMUR PLASMAP.F6N L
04046963361952COLUMBUS CR NARROW FEMUR PLASMAP.F5N L
04046963361945COLUMBUS CR NARROW FEMUR PLASMAP.F4N L

© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.