DVR® CROSSLOCKPLATE, STANDARD RIGHT WITH SMOOTH PEGS 811912050

GUDID 00887868076961

Biomet Orthopedics, LLC

Orthopaedic fixation plate kit, non-bioabsorbable, sterile Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial

• Primary Device ID: 00887868076961
• NIH Device Record Key: 212ce091-c1d3-4082-aa83-bddbae935117
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DVR® CROSSLOCKPLATE, STANDARD RIGHT WITH SMOOTH PEGS
• Version Model Number: 811912050
• Catalog Number: 811912050
• 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
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868076961 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112345

FDA Product Code

• LXT: APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-24

Devices Manufactured by Biomet Orthopedics, LLC

• 00887868004087 - PRIMARY TREPHINE: 2024-04-03
• 00887868004094 - BUSHING: 2024-04-03
• 00887868004100 - SECONDARY TREPHINE: 2024-04-03
• 00887868048272 - TREPHINE: 2024-04-03
• 00887868048289 - TREPHINE: 2024-04-03
• 00887868048296 - TREPHINE: 2024-04-03
• 00887868048302 - TREPHINE: 2024-04-03
• 00880304658387 - Compress®: 2024-03-11