IMF SYSTEM 91-5311

GUDID 00841036084783

BIOMET MICROFIXATION, INC

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 00841036084783
• NIH Device Record Key: 09782f13-c4d0-4a1d-beea-81bf794a99ca
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: IMF SYSTEM
• Version Model Number: 91-5311
• Catalog Number: 91-5311
• Company DUNS: 046189866
• Company Name: BIOMET MICROFIXATION, INC
• 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: false
• 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(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM
• Phone: +1(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841036084783 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K040983

FDA Product Code

• DZE: IMPLANT, ENDOSSEOUS, ROOT-FORM

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00841036084783]

Moist Heat or Steam Sterilization

[00841036084783]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-10-11

On-Brand Devices [IMF SYSTEM]

• 00841036094133: 91-5305
• 00841036090784: 95-5307
• 00841036090777: 95-5305
• 00841036090760: 95-5309
• 00841036090715: 95-5311
• 00841036090692: 20-1199
• 00841036084806: 91-5307
• 00841036084790: 91-5309
• 00841036084783: 91-5311
• 00841036012175: 01-6875