Columbus® NN483

GUDID 04038653352593

COLUMBUS PATELLA 3-PEGS P3 33X9MM

Aesculap AG

Cruciate-retaining total knee prosthesis

• Primary Device ID: 04038653352593
• NIH Device Record Key: c844a8e4-ab48-4e28-8c68-fa0a0683a518
• Commercial Distribution Discontinuation: 2021-04-05
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Columbus®
• Version Model Number: NN483
• Catalog Number: NN483
• Company DUNS: 315018218
• Company Name: Aesculap AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com
• Phone: +1(888)229-3002
• Email: setworld_orders@aesculap.com

Device Dimensions

• Device Size Text, specify: 0
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Device Identifiers

Device Issuing Agency	Device ID
GS1	04038653352593 [Primary]

FDA Product Code

• JWH: PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2022-02-14
• Device Publish Date: 2015-09-24

On-Brand Devices [Columbus®]

• 04038653424795: COLUMBUS TIB.HEMI-SPACER T5 8MM RL/LM
• 04038653424788: COLUMBUS TIB.HEMI-SPACER T4/4+ 8MM RL/LM
• 04038653424771: COLUMBUS TIB.HEMI-SPACER T3/3+ 8MM RL/LM
• 04038653424764: COLUMBUS TIB.HEMI-SPACER T2/2+ 8MM RL/LM
• 04038653424740: COLUMBUS TIB.HEMI-SPACER T5 4MM RL/LM
• 04038653424733: COLUMBUS TIB.HEMI-SPACER T4/4+ 4MM RL/LM
• 04038653424726: COLUMBUS TIB.HEMI-SPACER T3/3+ 4MM RL/LM
• 04038653424719: COLUMBUS TIB.HEMI-SPACER T2/2+ 4MM RL/LM
• 04038653424627: COLUMBUS TIB.HEMI-SPACER T3/3+ 4MM RM/LL
• 04038653445752: COLUMBUS TIB.HEMI-SPACER T0/0+ 8MM RL/LM
• 04038653445745: COLUMBUS TIB.HEMI-SPACER T0/0+ 4MM RL/LM
• 04038653424757: COLUMBUS TIB.HEMI-SPACER T1/1+ 8MM RL/LM
• 04038653424665: COLUMBUS TIB.HEMI-SPACER T2/2+ 8MM RM/LL
• 04038653424641: COLUMBUS TIB.HEMI-SPACER T5 4MM RM/LL
• 04038653424634: COLUMBUS TIB.HEMI-SPACER T4/4+ 4MM RM/LL
• 04038653424610: COLUMBUS TIB.HEMI-SPACER T2/2+ 4MM RM/LL
• 04038653424702: COLUMBUS TIB.HEMI-SPACER T1/1+ 4MM RL/LM
• 04038653424603: COLUMBUS TIB.HEMI-SPACER T1/1+ 8MM RM/LL
• 04038653445721: COLUMBUS TIB.HEMI-SPACER T0/0+ 4MM RM/LL
• 04038653445738: COLUMBUS TIB.HEMI-SPACER T0/0+ 8MM RM/LL
• 04038653424696: COLUMBUS TIB.HEMI-SPACER T5 8MM RM/LL
• 04038653424689: COLUMBUS TIB.HEMI-SPACER T4/4+ 8MM RM/LL
• 04038653424672: COLUMBUS TIB.HEMI-SPACER T3/3+ 8MM RM/LL
• 04038653424597: COLUMBUS TIB.HEMI-SPACER T1/1+ 4MM RM/LL
• 04038653352609: COLUMBUS PATELLA 3-PEGS P4 36X10MM
• 04038653352593: COLUMBUS PATELLA 3-PEGS P3 33X9MM
• 04038653352586: COLUMBUS PATELLA 3-PEGS P2 30X8MM
• 04038653352579: COLUMBUS PATELLA 3-PEGS P1 27X7MM
• 04038653352265: TIBIA EXTENSION STEM D14MM SHORT