General Instrument

GUDID 00817701028062

Nextremity 2.0mm x 4" K-Wire Sterile

NEXTREMITY SOLUTIONS, INC.

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• Primary Device ID: 00817701028062
• NIH Device Record Key: feb301a3-4675-499a-a5bb-690d009a6cbc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: General Instrument
• Version Model Number: NSI-KW20
• Company DUNS: 060783407
• Company Name: NEXTREMITY SOLUTIONS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817701028062 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-05-05
• Device Publish Date: 2020-11-10

On-Brand Devices [General Instrument]

• 00817701028079: Lapidus Cut Guide
• 00817701028062: Nextremity 2.0mm x 4" K-Wire Sterile