2.7MM SYSTEM SP-2843

GUDID 00888233019231

BIOMET MICROFIXATION, INC

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 00888233019231
• NIH Device Record Key: 1f439be4-685f-415c-87e9-bff83db63c7d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: 2.7MM SYSTEM
• Version Model Number: SP-2843
• Catalog Number: SP-2843
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00888233019231 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K854886

FDA Product Code

• JEY: PLATE, BONE

Sterilization

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

[00888233019231]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-02-19
• Device Publish Date: 2020-06-16

On-Brand Devices [2.7MM SYSTEM]

• 00841036152710: SP-2843
• 00841036152697: SP-2842
• 00841036065638: CROSS-DRIVE EMERGENCY SCREW 3.2X16MM
• 00841036058579: CROSS-DRIVE EMERGENCY SCREW 3.2X12MM
• 00841036058562: CROSS-DRIVE EMERGENCY SCREW 3.2X10MM
• 00841036058555: CROSS-DRIVE EMERGENCY SCREW 3.2X8MM
• 00841036018399: DRILL 2.0X105MM 75MM STP J-NT
• 00841036018382: DRILL 2.0X70MM 40MM STP J-NT
• 00888233019231: SP-2843
• 00888233019217: SP-2842