PHOENIX ANTEGRADE NAIL SYSTEM 14-443440

GUDID 00887868096792

Biomet Orthopedics, LLC

Femur nail, sterile

• Primary Device ID: 00887868096792
• NIH Device Record Key: a626260d-a193-4369-b3d8-0563384e820d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PHOENIX ANTEGRADE NAIL SYSTEM
• Version Model Number: 14-443440
• Catalog Number: 14-443440
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	00887868096792 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072161

FDA Product Code

• HSB: ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

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

On-Brand Devices [PHOENIX ANTEGRADE NAIL SYSTEM]

• 00887868096891: 14-443540
• 00888480165545: 14-443744
• 00888480165453: 14-443736
• 00888480165422: 14-443734
• 00888480165255: 14-443644
• 00888480165231: 14-443642
• 00888480164180: 14-443246
• 00888480163923: 14-443146
• 00888480163886: 14-443142
• 00888480163763: 14-443130
• 00888480163749: 14-443128
• 00887868097119: 14-443742
• 00887868097072: 14-443738
• 00887868097065: 14-443732
• 00887868097041: 14-443648
• 00887868096990: 14-443640
• 00887868096983: 14-443638
• 00887868096969: 14-443634
• 00887868096938: 14-443548
• 00887868096921: 14-443546
• 00887868096914: 14-443544
• 00887868096853: 14-443532
• 00887868096846: 14-443530
• 00887868096662: 14-443334
• 00887868096594: 14-443240
• 00887868096587: 14-443238
• 00887868096570: 14-443236
• 00887868096563: 14-443234
• 00887868096471: 14-443140
• 00887868096440: 14-443134
• 00887868096259: 14-443044
• 00887868096181: 14-443034
• 00887868096167: 14-443032
• 00888480165880: 14-443848
• 00888480165828: 14-443842
• 00888480165736: 14-443834
• 00888480165682: 14-443830
• 00888480165576: 14-443746
• 00887868097379: 14-443936
• 00887868097355: 14-443934
• 00887868097317: 14-443930
• 00887868097140: 14-443748
• 00887868097126: 14-443836
• 00888480165866: 14-443846
• 00888480165842: 14-443844
• 00888480165712: 14-443832
• 00888480164135: 14-443242
• 00888480164012: 14-443230
• 00888480163992: 14-443228
• 00888480163909: 14-443144