Crossfire 0475000010

GUDID 07613327145205

Upgrade USB Dongle, V. R.1.6

STRYKER CORPORATION

Arthroscopy information system application software

• Primary Device ID: 07613327145205
• NIH Device Record Key: 16c49036-94c2-43cf-b2e8-fcab08c43bd3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Crossfire
• Version Model Number: 0475000010
• Catalog Number: 0475000010
• Company DUNS: 187502109
• Company Name: STRYKER CORPORATION
• 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(866)624-4422
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327145205 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071859

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-23

On-Brand Devices [Crossfire]

• 07613327145205: Upgrade USB Dongle, V. R.1.6
• 07613327058109: 2 Console
• 07613327058093: Footswitch
• 07613327058086: Console