VANGUARD SSK360/DA360 KNEE SYSTEM 185268

GUDID 00880304481978

Biomet Orthopedics, LLC

Uncoated knee femur prosthesis, metallic

• Primary Device ID: 00880304481978
• NIH Device Record Key: 086660a5-eee3-4aa4-a243-cab28291d707
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VANGUARD SSK360/DA360 KNEE SYSTEM
• Version Model Number: 185268
• Catalog Number: 185268
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00880304481978 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093293

FDA Product Code

• MBV: Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer

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: 2019-12-11
• Device Publish Date: 2015-10-24

On-Brand Devices [VANGUARD SSK360/DA360 KNEE SYSTEM]

• 00880304482128: 185287
• 00880304482111: 185285
• 00880304482104: 185283
• 00880304482098: 185281
• 00880304482081: 185290
• 00880304482074: 185288
• 00880304482067: 185286
• 00880304482050: 185284
• 00880304482043: 185282
• 00880304482036: 185280
• 00880304482029: 185267
• 00880304482012: 185265
• 00880304482005: 185263
• 00880304481992: 185261
• 00880304481985: 185270
• 00880304481978: 185268
• 00880304481961: 185266
• 00880304481954: 185264
• 00880304481947: 185262
• 00880304467422: 185260