MATRIX MT2201

GUDID 03596010012302

MATRIX CEMENTED CUP X BAR

Smith & Nephew, Inc.

Orthopaedic prosthesis implantation instrument, reusable

• Primary Device ID: 03596010012302
• NIH Device Record Key: 3ec0be34-ed18-47ff-b217-f1a6faf5acef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MATRIX
• Version Model Number: MT2201
• Catalog Number: MT2201
• Company DUNS: 109903521
• Company Name: Smith & Nephew, Inc.
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com
• Phone: +1(800)821-5700
• Email: gudid@smith-nephew.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03596010012302 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P040033

FDA Product Code

• NXT: Prosthesis, hip, semi-constrained, metal/metal, resurfacing

Sterilization

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

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

[03596010012302]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-01-31
• Device Publish Date: 2015-10-05

On-Brand Devices [MATRIX]

• 00885556024966: MATRIX TREPHINE GUIDE TIP 12.5MM
• 03596010012197: MATRIX DISTAL SLEEVE REMOVAL ROD SIZE 10
• 03596010012180: MATRIX DISTAL SLEEVE REMOVAL ROD SIZE 8
• 03596010012043: MATRIX FEMORAL HEAD REMOVAL TOOL
• 03596010513229: MTX TR FEMORAL HEAD 36MM 14/16 +8
• 03596010512918: MTX TR FEMORAL HEAD 36 14/16 +0
• 03596010012401: MATRIX TRIAL FEMORAL HEAD 32MM OD +0MM
• 03596010012395: MATRIX TRIAL FEMORAL HEAD 28MM OD +8MM
• 03596010012388: MATRIX TRIAL FEMORAL HEAD 28MM OD +4MM
• 03596010012371: MATRIX TRIAL FEMORAL HEAD 28MM OD +0MM
• 03596010012333: MATRIX CEMENTED CUP PLACEMENT HEAD 32MM
• 03596010012326: MATRIX CEMENTED CUP PLACEMENT HEAD 28MM
• 03596010012319: MATRIX CEMENTED CUP PLACEMENT HEAD 22MM
• 03596010012302: MATRIX CEMENTED CUP X BAR
• 03596010012296: MATRIX CEMENTED CUP POSITIONER
• 03596010009791: MATRIX FEMORAL HEAD 22MMOD +12MM LENGTH
• 03596010009784: MATRIX FEMORAL HEAD 22MMOD +8MM LENGTH
• 03596010009777: MATRIX FEMORAL HEAD 22MMOD +4MM LENGTH
• 03596010009760: MATRIX FEMORAL HEAD 22MMOD +0MM LENGTH
• 03596010007391: MATRIX TITANIUM TAPER SLEEVE +12MM
• 03596010007384: MATRIX TITANIUM TAPER SLEEVE +0MM
• 03596010012425: DCU TRIAL FEMORAL HEAD 32MM OUTER DIAMETER +8MM
• 03596010012258: MATRIX TRIAL FEMORAL HEAD 22MM OD +0MM
• 03596010512901: MTX TR FEMORAL HEAD 36MM 14/16 +4
• 03596010012418: MATRIX TRIAL FEMORAL HEAD 32MM OD +4MM