ALLthread Titanium 902612

GUDID 00880304464544

Biomet Orthopedics, LLC

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 00880304464544
• NIH Device Record Key: a9dd1863-e47c-4c48-96c2-36b10ce653c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ALLthread Titanium
• Version Model Number: 902612
• Catalog Number: 902612
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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

Customer Support Contacts

• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304464544 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K042460

FDA Product Code

• GAT: SUTURE, NONABSORBABLE, SYNTHETIC, POLYETHYLENE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2020-05-11
• Device Publish Date: 2015-10-24

On-Brand Devices [ALLthread Titanium]

• 00880304563698: 902611
• 00880304563681: 902610
• 00880304465466: 902613
• 00880304464896: 902615
• 00880304464544: 902612
• 00880304464315: 902614
• 00880304464193: 902581
• 00880304464186: 902582
• 00880304453470: 902592
• 00880304453449: 902589
• 00880304453432: 902588
• 00880304444263: 902591