ALLTHREAD LACTOSORB 905942

GUDID 00880304445284

Biomet Orthopedics, LLC

Ligament reconstruction instrument set, reusable

• Primary Device ID: 00880304445284
• NIH Device Record Key: df89d703-5d74-4bb6-afd9-94cc0dfc82b9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ALLTHREAD LACTOSORB
• Version Model Number: 905942
• Catalog Number: 905942
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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	00880304445284 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K061389

FDA Product Code

• HWC: Screw, fixation, bone

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-02-21
• Device Publish Date: 2015-10-24

On-Brand Devices [ALLTHREAD LACTOSORB]

• 00880304481206: 905945
• 00880304452480: 905943
• 00880304450325: 905941
• 00880304449954: 905940
• 00880304445284: 905942
• 00880304445130: 905944