Polaris 20-8000-070-19

GUDID 00889024305045

Orthosoft Inc

Electrical-only medical device connection cable, reusable

• Primary Device ID: 00889024305045
• NIH Device Record Key: a98ac125-aa14-462c-bc3b-3ff9e02608c4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Polaris
• Version Model Number: 20-8000-070-19
• Catalog Number: 20-8000-070-19
• Company DUNS: 205670032
• Company Name: Orthosoft 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)-348-2759
• Email: zimmer.consumerrelations@zimmer.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024305045 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071714

FDA Product Code

• HAW: Neurological Stereotaxic Instrument

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: 2016-09-14

On-Brand Devices [Polaris]

• 00889024305045: 20-8000-070-19
• 00889024305021: 20-8000-070-08