NEO CLASSIC™ 20-8012-010-37

GUDID 00889024430174

SYNVASIVE TECHNOLOGY, INC.

Knee arthroplasty force sensor balance kit

• Primary Device ID: 00889024430174
• NIH Device Record Key: 2dc77d9b-589e-4323-a20c-cae419bfbe86
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NEO CLASSIC™
• Version Model Number: 20-8012-010-37
• Catalog Number: 20-8012-010-37
• Company DUNS: 618258974
• Company Name: SYNVASIVE TECHNOLOGY, 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: 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 Dimensions

• Height: 11 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889024430174 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00889024430174]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-07-07

On-Brand Devices [NEO CLASSIC™]

• 00889024430273: 20-8012-010-47
• 00889024430266: 20-8012-010-46
• 00889024430259: 20-8012-010-45
• 00889024430242: 20-8012-010-44
• 00889024430235: 20-8012-010-43
• 00889024430228: 20-8012-010-42
• 00889024430211: 20-8012-010-41
• 00889024430204: 20-8012-010-40
• 00889024430198: 20-8012-010-39
• 00889024430181: 20-8012-010-38
• 00889024430174: 20-8012-010-37
• 00889024430167: 20-8012-010-36
• 00889024430150: 20-8012-010-35
• 00889024430143: 20-8012-010-34
• 00889024430136: 20-8012-010-33