MaxFuse VBR, 10 (D) x 12 (W) x 25 (H) 62-1012-38

GUDID 00846468055042

10 (D) x 12 (W) x 25 (H)

Pioneer Surgical Technology, Inc.

Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis Vertebral body prosthesis

• Primary Device ID: 00846468055042
• NIH Device Record Key: 6ac5bbbf-a6ef-43b8-8c6d-431dfeddbb96
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MaxFuse VBR, 10 (D) x 12 (W) x 25 (H)
• Version Model Number: 62-1012-38
• Catalog Number: 62-1012-38
• Company DUNS: 793384496
• Company Name: Pioneer Surgical Technology, 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: false
• 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	00846468055042 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131724

FDA Product Code

• MQP: SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-24
• Device Publish Date: 2015-11-30

On-Brand Devices [MaxFuse VBR, 10 (D) x 12 (W) x 25 (H)]

• 00846468055059: 62-1012-39
• 00846468055042: 10 (D) x 12 (W) x 25 (H)