SIDEKICK

GUDID 00840420127945

WRIGHT MEDICAL TECHNOLOGY, INC.

External orthopaedic fixation system, reusable

• Primary Device ID: 00840420127945
• NIH Device Record Key: 0583be42-7e04-4bd7-9274-f9f0fd42d2eb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SIDEKICK
• Version Model Number: RR1205CE
• Company DUNS: 807201207
• Company Name: WRIGHT MEDICAL TECHNOLOGY, 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com

Device Dimensions

• Lumen/Inner Diameter: 120 Millimeter
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0
• Lumen/Inner Diameter: 120 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840420127945 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K052005

FDA Product Code

• KTT: APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

Sterilization

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

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

[00840420127945]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-01

On-Brand Devices [SIDEKICK]

• 00840420185266: RR20PF
• 00840420185259: RR20P
• 00840420166180: RR2401
• 00840420153319: RR007DRS
• 00840420152305: RR109
• 00840420143365: RR108
• 00840420143280: RR1203
• 00840420143273: RR007DLS
• 00840420142740: RR5300C
• 00840420137340: RR302580
• 00840420137265: RR3030
• 00840420137234: RR1450
• 00840420137227: RR5300
• 00840420137173: RR5200
• 00840420137142: RR180DFP
• 00840420137135: RR160DFP
• 00840420137128: RR140DFP
• 00840420137111: RR120DFP
• 00840420137104: RR200FP
• 00840420137098: RR180FP
• 00840420137074: RR20058
• 00840420137067: RR18058
• 00840420137050: RR16058
• 00840420137043: RR14058
• 00840420137036: RR1805
• 00840420137029: RR1605
• 00840420137012: RR1405
• 00840420137005: RR180
• 00840420136992: RR160
• 00840420136985: RR140
• 00840420136978: RR120
• 00840420136961: RR5100
• 00840420136954: RR4100
• 00840420128980: XP320100
• 00840420128782: RRTM0001
• 00840420128775: RRCF0180
• 00840420128768: RRCF0160
• 00840420128751: RRCF0140
• 00840420128744: RRCF0120
• 00840420128737: RR7500
• 00840420128720: RR717060
• 00840420128713: RR712525
• 00840420128706: RR6025TN
• 00840420128690: RR5300W
• 00840420128683: RR5300P
• 00840420128676: RR5050TN
• 00840420128669: RR5040TN
• 00840420128652: RR5040
• 00840420128645: RR5035TN
• 00840420128638: RR5030TN