M2A-MAGNUM HIP SYSTEM CP156432

GUDID 00880304656390

Biomet Orthopedics, LLC

Metallic femoral head prosthesis

• Primary Device ID: 00880304656390
• NIH Device Record Key: ed79377f-c544-459d-9aa0-735795aaab89
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: M2A-MAGNUM HIP SYSTEM
• Version Model Number: CP156432
• Catalog Number: CP156432
• 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

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304656390 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K062997

FDA Product Code

• LZO: Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

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: 2016-02-01

On-Brand Devices [M2A-MAGNUM HIP SYSTEM]

• 00880304656437: CP156436
• 00880304656420: CP156435
• 00880304656413: CP156434
• 00880304656406: CP156433
• 00880304656390: CP156432
• 00880304656383: CP156431