Wizard CaP

GUDID 00868201000140

Calcium compound bone void filler (5 cc)

Vivorte, Inc

Bone matrix implant, synthetic, non-antimicrobial

• Primary Device ID: 00868201000140
• NIH Device Record Key: 3d3f8513-ca24-4ae5-af9a-3e0ed4777214
• Commercial Distribution Discontinuation: 2021-07-29
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Wizard CaP
• Version Model Number: 5 cc
• Company DUNS: 078400984
• Company Name: Vivorte, 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00868201000140 [Primary]

FDA Product Code

• MQV: Filler, Bone Void, Calcium Compound

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-08-06
• Device Publish Date: 2021-07-29

On-Brand Devices [Wizard CaP]

• 00868201000157: Calcium compound bone void filler (10 cc)
• 00868201000140: Calcium compound bone void filler (5 cc)
• 00868201000133: Calcium Bone Void Filler (3 cc)