G7 PROVISIONAL APICAL LOCKING SCREW 110010237

GUDID 00880304568648

Biomet Orthopedics, LLC

Orthopaedic implant/trial-implant holder, reusable

• Primary Device ID: 00880304568648
• NIH Device Record Key: 4874aede-1999-452b-b073-cb338d4276c0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: G7 PROVISIONAL APICAL LOCKING SCREW
• Version Model Number: 110010237
• Catalog Number: 110010237
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 10
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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(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
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304568648 [Primary]
GS1	70880304568647 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121874

FDA Product Code

• OQG: Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented

Sterilization

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

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

[00880304568648]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-10-26

On-Brand Devices [G7 PROVISIONAL APICAL LOCKING SCREW]

• 00880304568648: 110010237
• 00880304540194: 010002601