Vanguard® Knee System 184790

GUDID 00887868344176

Biomet Orthopedics, LLC

Polyethylene patella prosthesis

• Primary Device ID: 00887868344176
• NIH Device Record Key: 2cbb072a-432c-47f1-86f9-7e137f16133a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vanguard® Knee System
• Version Model Number: 184790
• Catalog Number: 184790
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	00887868344176 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K110362

FDA Product Code

• OIY: Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive

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: 2019-10-21
• Device Publish Date: 2019-10-11

On-Brand Devices [Vanguard® Knee System]

• 00887868344220: 184795
• 00887868344213: 184794
• 00887868344206: 184793
• 00887868344190: 184792
• 00887868344183: 184791
• 00887868344176: 184790
• 00887868344169: 184788
• 00887868344152: 184786
• 00887868344145: 184784
• 00887868344138: 184782
• 00887868344121: 184780
• 00887868344114: 184770
• 00887868344107: 184768
• 00887868344091: 184766
• 00887868344084: 184764
• 00887868344077: 184762
• 00887868344060: 184760
• 00887868344053: 184728
• 00887868344046: 184726
• 00887868344039: 184724
• 00887868344022: 184722
• 00887868344015: 184720
• 00887868344008: 184710
• 00887868343995: 184708
• 00887868343988: 184706
• 00887868343971: 184704
• 00887868343964: 184702
• 00887868343957: 184700
• 00887868227592: 183099
• 00887868246555: 183621
• 00880304653450: CP113593
• 00880304653443: CP113592