Columbus® REVISION NR261K

GUDID 04046963339630

COLUMBUS TIB.HEMI-SPCR.T5 10MM RL/LM

Aesculap AG

Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge Knee arthroplasty wedge
Primary Device ID04046963339630
NIH Device Record Key057e9919-2c2e-4f55-ad6d-3c43c1161861
Commercial Distribution StatusIn Commercial Distribution
Brand NameColumbus® REVISION
Version Model NumberNR261K
Catalog NumberNR261K
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

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Device Identifiers

Device Issuing AgencyDevice ID
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [Primary]
GS104046963339630 [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® REVISION]

04046963339647COLUMBUS TIB.HEMI-SPCR.T5 15MM RL/LM
04046963339630COLUMBUS TIB.HEMI-SPCR.T5 10MM RL/LM
04046963339623COLUMBUS TIB.HEMI-SPCR.T5 5MM RL/LM
04046963339609COLUMBUS TIB.HEMI-SPCR.T4/4+ 15MM RL/LM
04046963339593COLUMBUS TIB.HEMI-SPCR.T4/4+ 10MM RL/LM
04046963339586COLUMBUS TIB.HEMI-SPCR.T4/4+ 5MM RL/LM
04046963339562COLUMBUS TIB.HEMI-SPCR.T3/3+ 15MM RL/LM
04046963339555COLUMBUS TIB.HEMI-SPCR.T3/3+ 10MM RL/LM
04046963339548COLUMBUS TIB.HEMI-SPCR.T3/3+ 5MM RL/LM
04046963339524COLUMBUS TIB.HEMI-SPCR.T2/2+ 15MM RL/LM
04046963339517COLUMBUS TIB.HEMI-SPCR.T2/2+ 10MM RL/LM
04046963339500COLUMBUS TIB.HEMI-SPCR.T2/2+ 5MM RL/LM
04046963339487COLUMBUS TIB.HEMI-SPCR.T1/1+ 15MM RL/LM
04046963339470COLUMBUS TIB.HEMI-SPCR.T1/1+ 10MM RL/LM
04046963339449COLUMBUS TIB.HEMI-SPCR.T0/0+ 15MM RL/LM
04046963339425COLUMBUS TIB.HEMI-SPCR.T0/0+ 5MM RL/LM
04046963338022COLUMBUS TIB.HEMI-SPCR.T4/4+ 15MM RM/LL
04046963338008COLUMBUS TIB.HEMI-SPCR.T4/4+ 5MM RM/LL
04046963337926COLUMBUS TIB.HEMI-SPCR.T2/2+ 5MM RM/LL
04046963337902COLUMBUS TIB.HEMI-SPCR.T1/1+ 15MM RM/LL
04046963337896COLUMBUS TIB.HEMI-SPCR.T1/1+ 10MM RM/LL
04046963337858COLUMBUS TIB.HEMI-SPCR.T0/0+ 10MM RM/LL

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