PHOENIX ANKLE NAIL SYSTEM 14-440071

GUDID 00887868093494

Biomet Orthopedics, LLC

Bone nail end-cap, sterile

• Primary Device ID: 00887868093494
• NIH Device Record Key: 3fe7923e-9cfa-4083-8528-da184c948d5e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PHOENIX ANKLE NAIL SYSTEM
• Version Model Number: 14-440071
• Catalog Number: 14-440071
• 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 Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868093494 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081243

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: 4
• Public Version Date: 2018-10-22
• Device Publish Date: 2015-10-24

On-Brand Devices [PHOENIX ANKLE NAIL SYSTEM]

• 00887868151279: 14-440030
• 00887868151262: 14-440021
• 00887868097652: 14-444180
• 00887868093708: 14-440330
• 00887868093692: 14-440327
• 00887868093685: 14-440324
• 00887868093678: 14-440321
• 00887868093661: 14-440318
• 00887868093654: 14-440315
• 00887868093647: 14-440230
• 00887868093630: 14-440227
• 00887868093623: 14-440224
• 00887868093616: 14-440221
• 00887868093609: 14-440218
• 00887868093593: 14-440215
• 00887868093586: 14-440130
• 00887868093579: 14-440127
• 00887868093562: 14-440124
• 00887868093555: 14-440121
• 00887868093548: 14-440118
• 00887868093531: 14-440115
• 00887868093524: 14-440074
• 00887868093517: 14-440073
• 00887868093500: 14-440072
• 00887868093494: 14-440071
• 00887868093180: 14-440015