AIM™SUPRACONDYLAR NAIL 800212015

GUDID 00887868031403

Biomet Orthopedics, LLC

Femur nail, sterile Femur nail Femur nail Femur nail Femur nail Femur nail Femur nail Femur nail Femur nail

• Primary Device ID: 00887868031403
• NIH Device Record Key: 663b1e87-d3d5-44c1-95c8-268193a20750
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AIM™SUPRACONDYLAR NAIL
• Version Model Number: 8002-12-015
• Catalog Number: 800212015
• 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	00887868031403 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K974781

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 [AIM™SUPRACONDYLAR NAIL]

• 00887868005336: 1812-30
• 00887868005329: 1812-25
• 00887868005312: 1812-20
• 00887868005305: 1812-15
• 00887868005299: 1810-30
• 00887868005282: 1810-25
• 00887868005275: 1810-20
• 00887868005268: 1810-15
• 00887868031434: 8002-12-030
• 00887868031427: 8002-12-025
• 00887868031410: 8002-12-020
• 00887868031403: 8002-12-015
• 00887868031397: 8002-10-030
• 00887868031380: 8002-10-025
• 00887868031373: 8002-10-020
• 00887868031366: 8002-10-015